The translation of this document is outdated.
Translation validity: 03.01.2024.–21.11.2024.
Amendments not included:
14.11.2024.
Text consolidated by Valsts valodas centrs (State
Language Centre) with amending laws of:
26 February 1998 [shall
come into force on 12 March 1998];
1 June 2000 [shall come into force on 28 June
2000];
20 June 2001 [shall come into force on 20 July
2001];
25 March 2004 [shall come into force on 22 April
2004];
27 May 2004 [shall come into force on 30 June
2004];
16 June 2005 [shall come into force on 20 July
2005];
8 June 2006 [shall come into force on 11 July
2006];
1 March 2007 [shall come into force on 29 March
2007];
27 September 2007 [shall come into force on 5 October
2007];
8 November 2007 [shall come into force on 1 January
2007];
8 May 2008 [shall come into force on 11 June 2008];
8 April 2009 [shall come into force on 13 May
2009];
18 June 2009 [shall come into force on 1 July
2009];
1 December 2009 [shall come into force on 1 January
2010];
10 December 2009 [shall come into force on 1 March
2010];
1 June 2010 [shall come into force on 1 January
2011];
7 October 2010 [shall come into force on 1 January
2011];
31 March 2011 [shall come into force on 4 May
2011];
21 June 2012 [shall come into force on 25 July
2012];
18 April 2013 [shall come into force on 1 July
2013];
11 September 2014 [shall come into force on 15 October
2014];
18 June 2015 [shall come into force on 16 July
2015];
1 December 2016 [shall come into force on 22 December
2016];
8 June 2017 [shall come into force on 1 July 2017];
22 November 2017 [shall come into force on 1 January
2018];
15 May 2018 (Constitutional Court Judgment) [shall come
into force on 15 May 2018];
20 December 2018 [shall come into force on 1 January
2019];
21 May 2020 [shall come into force on 17 June
2020];
13 Janaury 2022 [shall come into force on 25 January
2022];
3 March 2022 [shall come into force on 5 March
2022];
21 April 2022 [shall come into force on 17 May
2022];
28 September 2023 [shall come into force on 1 January
2024];
6 December 2023 [shall come into force on 3 January
2024].
If a whole or part of a section has been amended, the
date of the amending law appears in square brackets at
the end of the section. If a whole section, paragraph or
clause has been deleted, the date of the deletion appears
in square brackets beside the deleted section, paragraph
or clause.
|
The Saeima1 has adopted and
the President has proclaimed the following law:
Medical Treatment Law
Chapter I
General Provisions
Section 1. The following terms are used in this
Law:
1) medical treatment - professional and individual
prophylaxis, diagnosis and medical treatment of diseases, medical
rehabilitation and care of patients;
2) medical practitioners - persons who have a medical
education and who are engaged in medical treatment;
3) medical treatment institutions - doctors' practices,
State and local government institutions, performers of economic
activity and commercial companies which are registered in the
Register of Medical Treatment Institutions conform with the
mandatory requirements for medical treatment institutions and
structural units thereof laid down in laws and regulations and
provide medical treatment services;
4) certificate of a medical practitioner - a document
issued by the Union of Professional Organisations of Medical
Practitioners of Latvia, the Latvian Medical Association, or the
Latvian Nurses Association that certifies the professional
proficiency of the relevant person and indicates that the medical
practitioner as a specialist is competent to independently engage
in the practice of medical treatment (specialist practice) in the
relevant field;
5) certification of a medical treatment institution -
activity of an independent third person certifying that the
medical treatment institution, its unit or services provided
conform to the requirements specified by the relevant
standards;
51) certificate of medical and diagnostic
methods - a document issued by the Union of Professional
Organisations of Medical Practitioners of Latvia, the Latvian
Medical Association, or the Latvian Nurses Association that
certifies the professional proficiency of the relevant person and
indicates that the medical practitioner in addition to the
competence specified thereto in laws and regulations is entitled
to independently apply the medical or diagnostic method indicated
in the certificate;
6) doctors' council - a meeting of not less than three
doctors in order to determine a diagnosis and further tactics of
medical treatment;
7) human infectious disease - a disease induced by an
infectious disease-causing agent the spread of which may cause an
epidemic (hereinafter - the infectious disease);
8) medical education - the aggregate of knowledge and
skills in the field of medicine conforming to an educational
programme accredited in accordance with the procedures laid down
in law which is certified by an educational document issued by an
educational institution;
9) medical technologies - methods to be applied in
medical treatment, medical devices, and medicinal products;
10) emergency medical assistance - assistance to
victims (persons who have been taken ill) in a critical state of
danger to life or health, provided by persons specially prepared
(trained, equipped) for such cases with relevant qualifications
in medicine who in accordance with such qualifications have legal
liability for their actions or omissions and the consequences of
such actions or omissions;
11) patient - a person who receives health care
services or seeks them;
12) care of patients - part of health care which is
directly or indirectly related to the maintenance, promotion,
protection, and recovery of health of the public, a family or a
person;
13) first aid - assistance provided to victims (persons
who have been taken ill) in a critical state of danger to life or
health by persons with or without medical qualifications, within
the scope of their knowledge and possibilities irrespective of
their proficiency and equipment;
14) medical rehabilitation - a field of medicine
dealing with the development or recovery of physical,
psychological, social, vocational, and educational potential of a
person in conformity with his or her physiological or anatomical
limitations or, in the case of stable health impairment, with the
adaptation of the life of a patient to the environment and
society;
15) [27 May 2004];
16) [21 June 2012];
17) improvement of professional qualifications - part
of post-graduate education in a specific profession or speciality
which occurs in accordance with a freely selected education
programme the content and time of acquisition of which is not
regulated;
18) mandatory requirements for medical treatment
institutions and their structural units - requirements the
observing of which shall be ensured by medical treatment
institutions or their structural units so that the provision of
medical assistance therein is permitted;
19) residency - employment relationship with a medical
treatment institution implementing an educational programme for
the education of an existing doctor in the acquisition in the
official language of a speciality in accordance with an
accredited professional residency educational programme in
medicine;
20) clinical guidelines - an aggregate of
evidence-based, classified, and updated recommendations for
decision-making support to medical practitioners and patients as
regards the most appropriate medical treatment in specific
clinical cases;
21) medical devices - any instrument, apparatus,
appliance, software, implant, reagent, material or other article
corresponding to the definition referred to in Article 2(1) of
Regulation (EU) 2017/745 of the European Parliament and of the
Council of 5 April 2017 on medical devices, amending Directive
2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No
1223/2009 and repealing Council Directives 90/385/EEC and
93/42/EEC;
22) psychiatric assistance - individual prophylaxis,
out-patient or in-patient diagnosis, medical treatment,
rehabilitation, and care for persons with mental health
disorders;
23) psychiatric assistance without the consent of the
patient - in-patient diagnosis, medical treatment,
rehabilitation, and care for persons with mental health disorders
without the consent of such person;
24) disaster medical system - an aggregate of State
coordinated measures which are taken by medical treatment
institutions and other institutions of the health care sector
irrespective of the form of ownership in order to save human
lives and to reduce the destructive impact on public health in
medical sector emergencies and public health emergencies;
25) medical treatment support person - a person who
does not have the right to engage in medical treatment but who is
directly involved in ensuring the health care process;
26) medical treatment support person certificate - a
document issued by the Union of Professional Organisations of
Medical Practitioners of Latvia which certifies the professional
preparedness of the relevant person and indicates that the
medical treatment support person is competent to become involved
in ensuring the health care process in a specific sector;
27) unified electronic information system of the health
sector (hereinafter - the health information system) - a
structured information system of the health sector which includes
individual information data sets of the health sectors and
ensures their unified operation;
28) team of emergency medical assistance - a mobile
unit for the provision of emergency medical assistance which
consists of the persons specified in laws and regulations and
which has an emergency medical vehicle at its disposal which
conforms to the requirements laid down in laws and
regulations;
29) telemedicine - provision of remote health care
service by using information and communication technologies. It
includes safe resending of medical data and information necessary
for medical treatment in the form of text, sound, pictures or
other;
30) in vitro diagnostic medical device - any medical
device, reagent, reagent product, calibrator, control material,
kit, instrument, apparatus, piece of equipment, software or
system corresponding to the definition referred to in Article
2(2) of Regulation (EU) 2017/746 of the European Parliament and
of the Council of 5 April 2017 on in vitro diagnostic medical
devices and repealing Directive 98/79/EC and Commission Decision
2010/227/EU.
31) palliative care - interdisciplinary, holistic care
of such patients whose illness is life-limiting and is not
susceptible to radical treatment, aiming to prevent or mitigate
the suffering caused by illness in order to ensure as high
quality of life for the patient as possible and support for his
or her family. Palliative care includes medical treatment and
prevention of the symptoms caused by illness, hospice care for
persons with the projected survival of up to six months,
psychological, social, and spiritual support, and also support
for the relatives of the patient during the mourning period after
the loss of the kin;
32) [Paragraph shall come into force on 1 July 2025 and
shall be included in the wording of the Regulation as of 1 July
2025 / See Paragraph 43 of Transitional
Provisions];
33) [Paragraph shall come into force on 1 July 2025 and
shall be included in the wording of the Regulation as of 1 July
2025 / See Paragraph 43 of Transitional
Provisions];
34) methodological management body - an institution or
its unit which develops unified principles for prophylaxis,
diagnosis, medical treatment and its succession in the relevant
field of health care, and also ensures systemic quality
monitoring of medical treatment processes in the State, carrying
out the methodological management of medical treatment
institutions in the relevant field of health care;
35) [Paragraph shall come into force on 1 July 2025 and
shall be included in the wording of the Regulation as of 1 July
2025 / See Paragraph 43 of Transitional
Provisions];
36) pharmacist - a health care specialist who has
obtained education corresponding to the requirements laid down in
the law On the Regulated Professions and the Recognition of
Professional Qualifications and provides health care services by
engaging in pharmacist's practice;
37) clinical pharmacist - a health care specialist who
has obtained education corresponding to the requirements laid
down in the law On the Regulated Professions and the Recognition
of Professional Qualifications in the field of pharmacy and has
acquired additional speciality in clinical pharmacy attested by a
higher education diploma for the acquisition of an accredited
study programme in clinical pharmacy and provides health care
services by engaging in pharmacist's practice.
[26 February 1998; 1 June 2000; 25 March 2004; 27 May 2004;
8 June 2006; 8 November 2007; 8 May 2008; 8 April 2009; 10
December 2009; 7 October 2010; 21 June 2012; 11 September 2014;
13 January 2022; 28 September 2023; 6 December 2023 /
Clause 34 shall come into force on 1 April 2024. See
Paragraphs 38 and 43 of the Transitional Provisions]
Section 2. The purpose of the Law is to govern public
relationships in medical treatment in order to ensure qualified
prophylaxis and diagnosis of diseases or injury, qualified
medical treatment and rehabilitation of patients, and to
determine special legal regulation provisions for economic
activity of medical treatment institutions.
[11 September 2014]
Section 3. (1) Health is physical, mental, and social
well-being, the natural basis of the existence and survival of
the State and the nation. Health care is the complex of measures
implemented by health care service providers, including
telemedicine and activities with medicinal products and medical
devices for ensuring, maintaining, and renewal of a patient's
health.
(2) The priority is health care of a pregnant woman, child and
person with foreseeable disability. The Cabinet shall determine
the procedures for the organisation, financing, and ensuring of
human resources of this priority.
[8 May 2008; 10 December 2009; 16 June 2010; 11 September
2014]
Section 4. (1) [22 November 2017 / See Paragraph 32 of
Transitional Provisions]
(2) A medical practitioner employed in local government
institutions, State and local government capital companies, and
public private capital companies who provides health care
services paid from the State budget in a medical treatment
institution which has entered into a contract for the payment for
the health care services provided shall receive remuneration in
accordance with the Law on Remuneration of Officials and
Employees of State and Local Government Authorities.
[27 May 2004; 16 June 2005; 8 June 2006; 1 December 2009;
22 November 2017]
Section 5. Everyone has a duty to take care of and
everyone is responsible for his or her own health, the health of
the nation, and the health of his or her relatives and
dependants.
Section 6.
[10 December 2009]
Chapter II
Supervision of Medical Treatment
Section 7. The Ministry of Welfare shall carry out
supervision of medical treatment and other institutions specified
in laws and regulations.
[25 March 2004]
Section 8. In the field of health care, the Ministry of
Welfare shall perform the following functions:
1) formulate State policy in the field of health care and
co-ordinate the implementation of such policy;
2) at the State level co-ordinate and manage the provision of
emergency medical care to victims in emergencies on a regional or
national scale;
3) [8 June 2006];
4) [27 May 2004];
5) [27 May 2004];
6) prepare and submit to the Cabinet for approval a list of
occupational diseases;
7) in co-operation with the Latvian Medical Association and
professional organisations of medical practitioners formulate
proposals of mandatory requirements for medical treatment
institutions and their structural units;
8) [8 June 2006];
9) [27 May 2004].
[1 June 2000; 25 March 2004; 27 May 2004; 8 June
2006]
Section 9. (1) The Cabinet shall determine the
procedures for developing, supplementing and maintaining
registers of medical practitioners, medical treatment support
persons, medical treatment institutions, and medical devices, and
of patients who are ill with certain diseases, newborns (with
details of their mothers), and also the procedures for approving
medical technologies to be used in medical treatment and the
procedures for introducing new medical technologies.
(11) [Paragraph shall come into force on 1
October 2024 and shall be included in the wording of the Law as
of 1 October 2024. See Paragraph 40 of Transitional
Provisions]
(2) The procedures for organising the disaster medical system
shall be determined by the Cabinet.
(3) The Cabinet shall determine the provision of a first aid
training system, the content of the provision of first aid
training programme, and the procedures for ensuring such
training.
(31) The Cabinet shall determine the manager of the
information system for the management of first aid training, the
amount of information to be included in this system and the
processing procedures thereof, and also the conditions for
ensuring access to the information included in the State
information system.
(4) In order to swiftly exchange the data on the resources
available at hospitals for ensuring the availability of
in-patient health care services and to monitor the severity and
outcome of disease for the admitted patients with infectious
diseases, the Cabinet shall determine the manager of the
information system for the resources of in-patient medical
treatment institutions, the data to be included in this
information system, the amount of such data, and the procedures
for processing them.
(5) The Cabinet shall determine the procedures for organising,
financing, and receiving palliative care.
(6) The Cabinet shall determine the criteria and procedures
for granting the status of a methodological management body, its
rights and obligations, and also the regulations for investing
public funds in a methodological management body.
(7) [Paragraph shall come into force on 1 July 2025 and
shall be included in the wording of the Law as of 1 July 2025 See
Paragraph 43 of Transitional Provisions]
[27 May 2004; 16 June 2005; 8 June 2006; 8 May 2008; 21
June 2012; 1 December 2016; 21 April 2022; 28 September 2023; 6
December 2023 / Paragraph six shall come into force on 1
April 2024. See Paragraph 38 of Transitional Provisions.
Amendment to Paragraph one regarding the deletion of the words
"medical practitioners, medical treatment support persons" and
Paragraph 1.1 shall come into force on 1 October 2024
and shall be included in the wording of the Law as of 1 October
2024. See Paragraph 40 of Transitional Provisions. Paragraph
seven shall come into force on 1 July 2025 and shall be included
in the wording of the Law as of 1 July 2025. See Paragraph 43 of
Transitional Provisions]
Section 9.1 (1) Medical treatment shall be
performed according to the clinical guidelines, clinical
algorithms, and clinical pathways or the safety and medical
efficiency evaluation of the use of the methods and medicinal
products to be used in medical treatment.
(2) The Cabinet shall determine the procedures for the
assessment, registration, introduction, and updating of clinical
guidelines, clinical algorithms, and clinical pathways.
[6 December 2023]
Section 9.2 (1) In cases when life is
endangered due to cardiac arrest until the moment when a team of
the State Emergency Medical Service arrives, a person may use the
automated external defibrillator for restoring the heartbeat of
the victim.
(2) The Cabinet shall determine:
1) the public spaces where automated external defibrillators
shall be installed and the requirements for the installation of
such defibrillators;
2) the procedures for the use and technical supervision of
automated external defibrillators;
3) [6 December 2023].
[21 April 2022; 6 December 2023]
Section 10. In medical treatment institutions, the
quality of professional health care and work disability
examination shall be controlled by the Health Inspectorate.
[27 May 2004; 27 September 2007]
Section 10.1 Contesting and appealing the
decisions of the Health Inspectorate which have been taken on the
failure to comply with the requirements of Sections 28, 33, and
35 of this Law shall not suspend the operation of these
decisions.
[21 May 2020 / Section shall come into force on 1 July
2020. See Paragraph 33 of Transitional Provisions]
Section 10.2 [Section shall come into
force on 1 July 2025 and shall be included in the wording of the
Law as of 1 July 2025. See Paragraph 43 of Transitional
Provisions]
Section 11. Advertisements and advertising related to
medical treatment, medical treatment institutions, and medical
practitioners shall be placed in the mass media in accordance
with the procedures laid down in laws and regulations.
Section 12. Persons who do not have medical education
and who are independently engaged in medical treatment of
patients, provision of assistance in deliveries (except in cases
where emergency assistance must be provided), hypnosis,
conditioning and other methods affecting the human psyche,
correction of the human energy field (bio-correction),
acupuncture, and other methods of affecting the energy system of
the human organism, as well as persons who provide support for
medical treatment activities by persons who do not have medical
education or do not have the right to practice a speciality shall
be subject to liability laid down in law.
Section 12.1 A medical practitioner is
entitled to get involved in the provision of health care process
if he or she is registered in the register of medical treatment
support persons.
[21 June 2012]
Chapter III
Medical Ethics Committee
Section 13. Medical ethics committees are advisory
bodies established for resolving problems of medical ethics which
operate in accordance with the model regulations approved by the
Cabinet.
Section 14. Medical ethics committees shall be
established by medical treatment institutions and professional
organisations of medical practitioners. Such committees shall
examine ethical matters related to the activities of medical
practitioners and new medical technologies.
Section 15. The Central Medical Ethics Committee shall
operate in accordance with Cabinet regulations and it shall
examine issues related to the ethics of biomedical progress
applicable to social problems. The Cabinet shall, upon
recommendation from the Minister for Welfare, approve members of
the Central Medical Ethics Committee.
[25 March 2004]
Section 15.1 When examining the issues
related to the ethics of biomedical progress applicable to social
problems, the Central Medical Ethics Committee shall apply a
price list of paid services. The price list of paid services
shall be approved by the Cabinet.
[6 December 2023]
Chapter IV
Rights and Responsibilities of Persons with Respect to Health
Care
[22 November 2017 / See Paragraph
32 of Transitional Provisions]
Section 16.
[22 November 2017 / See Paragraph 32 of Transitional
Provisions]
Section 17.
[22 November 2017 / See Paragraph 32 of Transitional
Provisions]
Section 18.
[22 November 2017 / See Paragraph 32 of Transitional
Provisions]
Section 19.
[8 June 2006]
Section 20.
[10 December 2009]
Section 21.
[10 December 2009]
Section 22.
[10 December 2009]
Section 23.
[10 December 2009]
Section 24.
[10 December 2009]
Section 25.
[10 December 2009]
Chapter V
Medical Practitioners and their Medical Treatment Activities
Section 26. (1) Medical practitioners who have been
registered in the medical practitioners register are permitted to
independently engage in medical treatment in the relevant
profession in conformity with the competence specified by the
Cabinet.
(2) Medical practitioners who have been certified and
registered with the medical practitioners register are permitted
to independently engage in medical treatment in a specific basic
speciality, sub-speciality or additional speciality (except for a
specific speciality of a nurse) in conformity with the competence
laid down by the Cabinet. Nurses who have been registered with
the medical practitioners register and have obtained an
educational document on the acquisition of the relevant
speciality are permitted to independently engage in medical
treatment in the specific speciality of a nurse in conformity
with the competence laid down by the Cabinet.
(3) Registered medical practitioners who have acquired an
educational programme conforming to the requirements laid down in
laws and regulations in relation to education necessary for
acquisition of the particular speciality have the right to apply
for a certificate of a medical practitioner in a specific
speciality. Registered medical practitioners who have acquired a
further education programme of the relevant medical treatment or
diagnostic method have the right to apply for a certificate of
medical treatment and diagnostic methods in a specific medical
treatment or diagnostic method.
(31) Medical practitioners who are registered and
have completed an educational programme in the relevant basic
speciality and certified medical practitioners who meet the
criteria specified in laws and regulations for the period of time
specified in laws and regulations have the right to apply for a
certificate of a medical practitioner in a newly created
additional speciality or sub-speciality, without completing the
educational programme referred to in Paragraph three of this
Section in a newly created additional speciality or
sub-speciality.
(4) A specific medical treatment or diagnostic method included
in the classification of medical treatment and diagnostic methods
may be independently applied by medical practitioners registered
in the register of medical practitioners (except for nurses) who
are certified in the relevant medical treatment or diagnostic
method. Nurses who have been registered with the medical
practitioners register are permitted to independently engage in
medical treatment in the relevant medical treatment or diagnostic
method if they have obtained an educational document certifying
that the relevant medical treatment or diagnostic method has been
acquired in practice as a nurse.
[8 May 2008; 21 June 2012; 1 December 2016; 13 January
2022]
Section 27. The competence of medical practitioners in
medical treatment and also the amount of theoretical and
practical knowledge, the criteria to be determined for medical
practitioners for obtaining the newly created additional
speciality or sub-speciality, without completing an educational
programme in the newly created additional speciality or
sub-speciality, and the period of time during which medical
practitioners who meet the specified criteria have the right to
apply for a certificate of a medical practitioner in the
aforementioned additional speciality or sub-speciality shall be
determined by the Cabinet, evaluating the opinion expressed by
the Latvian Medical Association, the Union of Professional
Organisations of Medical Practitioners of Latvia or the Latvian
Nurses Association in accordance with the competence.
[8 June 2006; 21 June 2012; 1 December 2016]
Section 28. [6 December 2023]
Section 29. (1) The right to practice a speciality
shall be certified by a certificate of a medical practitioner and
the registration of the person in accordance with the procedures
laid down in laws and regulations. The Cabinet shall determine
the procedures for organising the certification and
recertification of medical practitioners, the certification
examination and its course, and also the procedures for the
cancellation and suspending the validity of a certificate.
(11) In the process of certification of a medical
practitioner, the certification authority shall take the decision
to grant a certificate or to refuse to grant a certificate within
three months from the day of receiving an application. Due to
objective reasons, the certification authority may extend the
time period for taking the decision for a time period not
exceeding four months from the day of receiving the application,
notifying the submitter thereof.
(2) The certification of a medical practitioner in conformity
with their competence shall be performed by:
1) Latvian Medical Association - doctor and dentist
certification;
2) Union of Professional Organisations of Medical
Practitioners of Latvia - functional specialist, functional
specialist assistant, doctor's assistant, radiologist's
assistant, radiographer, masseur, cosmetician, laboratory
assistant, podologists, beauty care specialists (cosmetologists),
and dental technician certification;
3) Latvian Nurses Association - midwife and dental hygienist
certification.
(3) The list of medical treatment support person professions
to be certified and the procedures for certification shall be
determined by the Cabinet.
(4) The price list for the paid services of testing of the
professional knowledge, the preparation, registration, and
duplication of certificates of medical practitioners and medical
treatment support persons shall be approved by the Cabinet.
(5) [1 December 2016]
[1 June 2000; 8 May 2008; 8 April 2009; 21 June 2012; 11
September 2014; 1 December 2016; 13 January 2022; 6 December
2023]
Section 30.
[1 June 2000]
Section 31. Persons with a diploma of foreign medical
education shall acquire the right to engage in medical treatment
after recognition of the professional qualification of the
medical practitioner in accordance with the procedures laid down
in the law On the Regulated Professions and the Recognition of
Professional Qualifications.
[6 December 2023]
Section 32.
[1 June 2000]
Section 33. (1) Persons studying at medical education
institutions within the framework of the educational programme
may engage in medical treatment only under direct supervision of
a certified medical practitioner.
(2) The lists of the medical practitioners who have the right
to perform the teaching of students and medical practitioners, in
conformity with their competence shall be approved by the Latvian
Medical Association, the Union of Professional Organisations of
Medical Practitioners of Latvia or the Latvian Nurses
Association.
(21) Any doctor certified in a primary speciality,
sub-speciality, or additional speciality has the right to conduct
training of residents in a medical treatment institution
according to the educational programmes of residency accredited
in medicine.
(3) Students who have acquired the first or second level of a
professional higher medical education programme and the amount of
knowledge and skills of whom conforms to the specified
qualification and competence requirements may take part in
medical treatment. The qualification requirements and amount of
competence shall be determined by the Cabinet.
(4) The head of a medical treatment institution shall, if
necessary, employ a doctor studying in the primary speciality,
sub-speciality, or additional speciality to be acquired in
residency in the position of a doctor under supervision in
accordance with the procedures stipulated by the Cabinet.
[8 May 2008; 21 June 2012; 6 December 2023 / The new
wording of Paragraph three shall come into force on 1 October
2024 and shall be included in the wording of the Law as of 1
October 2024. See Paragraph 42 of Transitional
Provisions]
Section 34. (1) A head of a medical treatment
institution shall organise that such medical devices are used in
a medical treatment institution which comply with the laws and
regulations.
(2) The Cabinet shall determine:
1) the procedures for conducting clinical trials of medical
devices intended for human use and performance studies on in
vitro diagnostic medical devices;
2) essential requirements for medical devices and in vitro
diagnostic medical devices;
3) the procedures for recycling single-use medical devices and
also the procedures by which medical devices and in vitro
diagnostic medical devices shall be placed on the market and put
into service (introduced);
4) the procedures for the registration of information on
manufacturers of medical devices and in vitro diagnostic medical
devices, medical devices and in vitro diagnostic medical devices
manufactured by them, and also distributors of medical devices
and in vitro diagnostic medical devices;
5) the procedures for the distribution and operation of
medical devices and in vitro diagnostic medical devices, and also
vigilance, post-market and technical surveillance.
(3) The quality and safety standards for the collection,
testing, processing, storage, and distribution of human blood and
blood components, import and export conditions, and also
compensation for expenditures for the renewal of the lost volume
of blood shall be determined by the Cabinet.
(4) A sponsor of clinical trials of medical devices intended
for human use and performance studies of in vitro diagnostic
medical devices has an obligation to insure his or her civil
legal liability and also that of his or her researchers for the
damage inflicted on the health or life of the subject within the
scope of clinical trials of medical devices intended for human
use and performance studies on in vitro diagnostic medical
devices.
(5) Civil liability insurance shall cover the entire duration
of clinical trials of medical devices intended for human use and
performance studies on in vitro diagnostic medical devices. A
civil liability insurance contract shall be entered in relation
to each individual clinical trial of medical devices intended for
human use and performance study on in vitro diagnostic medical
devices prior to the commencement of the relevant trial or
study.
(6) The Cabinet shall determine the procedures for the civil
liability insurance of a sponsor of clinical trials of medical
devices intended for human use and performance studies on in
vitro diagnostic medical devices and a medical treatment
institution, the minimum limit of liability of the insurance
contract, and the mandatory risks to be insured by the sponsor of
clinical trials of medical devices intended for human use and
performance studies on in vitro diagnostic medical devices.
[1 June 2000; 16 June 2005; 8 June 2006; 13 January 2022; 3
March 2022; 6 December 2023]
Section 35. A head of a medical treatment institution
shall be held liable in accordance with the procedures laid down
in law if the institution managed by him or her uses medical
technologies that have not been approved in accordance with the
procedures prescribed by the Cabinet.
[1 June 2000; 25 March 2004; 27 May 2004]
Section 36. Medical practitioners shall be held liable
for the use of selected medical technology and consequences
caused by it.
[1 June 2000]
Chapter VI
Profession of Doctor
Section 37. (1) A doctor is a medical practitioner who
has acquired an education which conforms to the requirements laid
down in the law On the Regulated Professions and the Recognition
of Professional Qualifications and who, with scientifically
grounded medical activities, directly or indirectly affects
humans and within the scope of his or her professional
activities:
1) performs illness prophylaxis, diagnosis, medical treatment,
and medical rehabilitation of the patient;
2) evaluates illnesses and the functional restrictions caused
by them at the level of body, activity, and participation;
3) investigates the origin of illnesses and the prophylactic
possibilities.
(2) [ 8 May 2008]
[8 June 2006; 8 May 2008; 11 June 2008 / See Transitional
Provisions]
Section 38. A doctor shall be independent in his or her
professional activities. All doctors have the right to provide an
opinion on the state of health and treatment of a patient.
Section 39. A doctor shall engage in a speciality
(there may be several specialities) specified in his or her
doctor's certificate. A doctor may engage in a sub-speciality,
additional speciality or use a particular examination or
treatment method only if he or she has a doctor's certificate in
the primary speciality.
[1 June 2000]
Section 39.1 If necessary, the head of a
medical treatment institution may, in ensuring health care,
employ a doctor under supervision who may be engaged in medical
treatment in primary speciality, sub-speciality, additional
speciality or may use the medical treatment or diagnostic method
in which he or she has completed a residency programme or in
which he or she has been certified only under the management of a
specialist certified in the relevant speciality or medical
treatment or diagnostic method. A doctor, except for the doctor
referred to in Section 33, Paragraph four, may work in the
position of a doctor under supervision for not longer than five
years (including in total) throughout his or her professional
activity.
[6 December 2023]
Section 40. A doctor has a duty to protect unborn life
and he or she has a duty to try to dissuade a pregnant woman from
terminating pregnancy if the pregnancy is not in contradiction
with the woman's state of health and if there is no danger that
the newborn will have an inherited or acquired disease. A doctor
has the right to refuse to terminate a pregnancy if there are no
medical grounds for such termination.
Section 41.
[10 December 2009]
Section 42. In cases where the life of a patient is not
endangered but the patient does not observe the specified
regimen, does not comply with instructions of the medical
practitioners or knowingly harms his or her health and thus
directly affects the medical treatment of the specific disease,
the doctor has the right to refuse further treatment of the
patient.
Section 43. A doctor may examine or treat a patient
jointly with other medical practitioners or not permit their
participation.
Chapter VI A
Profession of Dentist
[25 March 2004]
Section 43.1 A dentist is a medical
practitioner who has acquired an education which conforms to the
requirements laid down in the law On the Regulated Professions
and the Recognition of Professional Qualifications and who within
the scope of his or her professional activities:
1) performs prophylaxis, diagnosis, and medical treatment of
alveolar outgrowths and oral cavity mucous membrane, jaws and the
tissue illnesses associated thereof;
2) investigates the origins and prophylactic possibilities of
the illnesses referred to in Clause 1 of this Section.
Section 43.2 If necessary, the head of a
medical treatment institution may employ a doctor under
supervision who may be engaged in medical treatment in primary
speciality, sub-speciality in which he or she has completed a
dentistry study programme or a residency educational programme of
sub-speciality or in which he or she has been certified only
under the management of a dentist certified in the relevant
speciality. A dentist may work in the position of a doctor under
supervision for not longer than five years (including in total)
throughout his or her professional activity.
[6 December 2023]
Chapter VII
Nurses and Profession of Doctor's Assistant
[11 September 2014]
Section 44. (1) A nurse is a medical practitioner who
has acquired an education in conformity with the requirements
laid down in the law On the Regulated Professions and the
Recognition of Professional Qualifications.
(2) A nurse within the framework of professional activity in
conformity with the competence thereof shall:
1) provide patient care;
2) participate in medical treatment;
3) manage the work of providing care to patients;
4) work with education of patients in matters of health;
5) perform professional education work.
Section 45. (1) A doctor's assistant is a medical
practitioner who has acquired a secondary professional education
or first level higher professional education, or higher education
in conformity with an accredited doctor's assistant study
programme.
(2) A doctor's assistant within the framework of professional
activity in conformity with the competence thereof shall carry
out professional and individual diagnosing and medical treatment
and also in co-operation with a doctor ensure preventive
measures.
Chapter VII A
Functional Specialist and Assistant to a Functional
Specialist
[20 June 2001]
Section 45.1 (1) A functional specialist
(physiotherapist, occupational therapist, technical orthopaedist,
audio speech therapist, nutritional specialist, art therapist,
optometrist) is a medical practitioner who has acquired a second
level vocational higher medical education and operates according
to his or her competence in medical treatment.
(2) An assistant to a functional specialist (an assistant to a
physiotherapist, an assistant to an occupational therapist) is a
medical practitioner who has acquired a higher medical education
at the first level or at least at the third professional
qualification level and acts according to his or her competence
in medical treatment.
[8 June 2006; 8 May 2008; 21 June 2012; 1 December 2016
/ The amendment to Paragraph one regarding the supplementation
thereof with the word "optometrist" shall come into force on 1
January 2020. See Paragraph 23 of Transitional
Provisions]
Section 45.2 (1) In his or her speciality, a
functional specialist within the scope of his or her professional
competence shall:
1) understand the evaluation of human functional limitations
and rehabilitation principles;
2) perform medical treatment by using appropriate diagnostics,
evaluation, and medical technologies, and shall provide
opinions;
3) perform professional education work.
(2) In his or her speciality, an assistant to a functional
specialist within the scope of his or her professional competence
shall:
1) understand the evaluation of human functional limitations
and rehabilitation principles;
2) perform medical treatment by making use of appropriate
medical technologies under the supervision of a functional
specialist or a doctor.
Chapter VII B
Profession of Midwife
[25 March 2004]
Section 45.3 A midwife is a medical
practitioner who has acquired an education which conforms to the
requirements laid down in the law On the Regulated Professions
and the Recognition of Professional Qualifications and who within
the scope of his or her professional activities shall:
1) ensure the physiological care of pregnancy, organise and
manage physiological birth and care after physiological birth,
and perform care of a healthy newborn;
2) having determined health risk factors or possible pathology
in the pregnant, natal, and postnatal women or newborn in his or
her care, send the patient to the relevant specialist doctor;
3) participate in medical treatment;
4) provide information and perform educational activities in
relation to family planning and contraception, pregnancy, natal
and postnatal, breast-feeding, sexual and reproductive health and
child care issues.
Chapter VII C
Profession of Military Paramedic
[31 March 2011]
Section 45.4 A military paramedic is a
medical practitioner who has acquired education conforming to the
requirements laid down in the law On the Regulated Professions
and the Recognition of Professional Qualifications and who, upon
fulfilling the duties of military service in and outside the
territory of Latvia, within the scope of his or her professional
activities shall:
1) evaluate the state of health of a patient;
2) provide emergency medical assistance.
Section 45.5 A military paramedic may
maintain his or her professional skills in providing emergency
medical assistance in the amount corresponding to his or her
qualification during military service in a team of an emergency
medical assistance institution under direct control and
supervision of a medical practitioner certified in emergency
medicine.
Chapter VII D
Profession of Masseur
[21 June 2012]
Section 45.6 A masseur is a medical
practitioner who has acquired first level vocational higher
education or vocational secondary education and acts according to
his or her competence in medical treatment.
Chapter VIII
Duties and Rights of Medical Practitioners in Medical
Treatment
Section 46. Medical practitioners have a duty to
provide first aid and emergency medical care.
Section 47. A medical practitioner has the right to
refuse first aid and emergency medical care in circumstances that
endanger the life of the medical practitioner himself or herself
and also where a medical practitioner is incapable of doing so
due to his or her state of health.
Section 48. A medical practitioner has a duty to
regularly improve professional qualifications and become educated
in the provision of emergency medical care. The Cabinet shall
determine the requirements in relation to further education and
also the procedures for the evaluation and approval of the
further education acquired.
[6 December 2023]
Section 49.
[10 December 2009]
Section 50.
[10 December 2009]
Section 51.
[10 December 2009]
Section 52.
[18 June 2009 / The amendment regarding the deletion of the
Section shall come into force on 1 October 2009. See Paragraph 16
of Transitional Provisions]
Section 53. A doctor, doctor's assistant, dentist, or
midwife shall determine temporary incapacity for work of a
person. The Cabinet shall determine the procedures for the
issuance and cancellation of the documents certifying temporary
incapacity for work.
[26 February 1998; 1 December 2016; 28 September
2023]
Section 53.1
[1 January 2022 / See Paragraph 29 of Transitional
Provisions]
Section 53.2 (1) In case of establishing a
trusteeship and future authorisation, the commission of medical
practitioners shall provide an opinion on whether a person has
lost the ability to understand the meaning of his or her actions
and to control them due to mental or health disorders.
(2) A statement on the basis of the opinion referred to in
Paragraph one of this Section may be requested by:
1) the future authorised person, presenting the future
authorisation;
2) the court in order to establish a trusteeship in accordance
with the procedures laid down in the Civil Procedure Law.
(3) A statement on the basis of the opinion referred to in
Paragraph one of this Section shall be issued by the head of the
medical treatment institution within 10 working days from the day
of receiving the request. If the statement is issued in relation
to a future authorisation, it shall be indicated in the statement
that it is intended for submission to the register of future
authorisations in order to record information in the register in
accordance with the procedures laid down in the Notariate
Law.
(4) The Cabinet shall determine the procedures by which a
medical treatment institution, in case of establishing a
trusteeship and future authorisation, shall establish a
commission of medical practitioners, by which the commission of
medical practitioners shall provide an opinion on the ability of
the person to understand the meaning of his or her actions and to
control them, by which the head of the medical treatment
institution shall issue a relevant statement on the basis of the
opinion, as well as the procedures for covering the costs of the
statement issued on the basis thereof.
[18 April 2013; 22 November 2017]
Chapter VIII A
Activity of a Pharmacist in Health Care and Cooperation with a
Medical Practitioner
[6 December 2023]
Section 53.3 A pharmacist and a clinical
pharmacist who works in a pharmacy or a closed-type pharmacy of a
medical treatment institution, or in a medical treatment
institution which does not have a closed-type pharmacy, shall
have the following tasks:
1) in providing pharmaceutical care, to ensure responsible,
safe, and rational use of medical products, medical devices, in
vitro diagnostic medical devices, and food supplements and
adherence in medical treatment;
2) in cooperation with medical practitioners, to form a
multidisciplinary team, participating in the development of the
pharmaco-therapeutic plan of the patient, its implementation and
monitoring in order for the patient to achieve the therapeutic
results, to mitigate the probable damage inflicted by the use of
medicinal products, and to improve health and also quality of
life;
3) to participate in the supervision of adverse effects to the
use of medicinal products;
4) to promote and ensure prophylactic health protection
measures.
[6 December 2023]
Section 53.4 In addition to that specified
in Section 53.3 of this Law, a clinical pharmacist
shall have the following tasks:
1) in cooperation with medical practitioners, to participate
in the determination of the pharmacotherapy for a patient, taking
into account the diagnosis, symptoms, and results of
examinations, and also safety, efficiency, and economical
principles in respect of indications, dosage, frequency and
duration of use of medicinal products;
2) to carry out direct supervision of the use of and adverse
effects to medicinal products by following the results of
examinations on regular basis, surveying the patient and
recording the supervision data and, where necessary, initiating
corrections of pharmacotherapy;
3) to provide consultations to medical practitioners
concerning pharmacokinetic, pharmacodynamic, and other issues
related to the prescription of medicinal products;
4) to participate in the organising and course of clinical
trials if such are conducted in a medical treatment
institution;
5) to participate in a systemic analysis of the use of
different means of medical treatment.
[6 December 2023]
Chapter IX
Medical Treatment Institutions
Section 54. (1) A medical treatment institution may be
established by State institutions, local governments, natural or
legal persons.
(2) Medical treatment institutions may be outpatient
institutions where patients, if placement in a hospital is not
necessary, are provided with medical treatment services, and
hospitals where patients who are under constant 24-hour care of
medical practitioners are provided with emergency medical
assistance, diagnosis, and medical treatment services until a
specific level of medical treatment is reached.
(3) For the provision of the medical treatment services
referred to in Paragraph two of this Section, a medical treatment
institution is entitled to provide the following services related
to the medicine until a specific level of medical treatment is
reached:
1) overnight accommodation which is provided to a patient and
a person who stays with the patient;
2) food which is provided to a patient;
3) transportation of a patient with a vehicle which is
specially equipped with medical devices.
[1 June 2000; 18 June 2009]
Section 54.1 (1) A university hospital shall
be a multi-profile in-patient medical treatment institution which
conforms to all of the following conditions:
1) provides patients with secondary and tertiary health care
services;
2) participates in the implementation of the bachelor's,
master's, residence, and doctoral study programmes and residency
programmes;
3) performs scientific and research work in the field of
medical treatment and promotes the introduction of new medical
treatment methods and medical technologies.
(2) The increased coefficient specified in laws and
regulations shall be applied to health care services paid for
from the State budget funds for the university hospital.
[1 December 2016 / Paragraph two shall come into force on 1
January 2020. See Paragraph 24 of Transitional
Provisions]
Section 55. (1) Only such medical treatment
institutions as conform to the mandatory requirements specified
for medical treatment institutions and their structural units may
engage in medical treatment.
(2) The Cabinet shall determine mandatory requirements for
medical treatment institutions and their structural units.
[1 June 2000; 8 April 2009]
Section 55.1 (1) In order to fulfil the
medical security tasks of the National Armed Forces, a medical
treatment institution of the National Armed Forces may establish
a temporary medical assistance point. A temporary medical
assistance point shall not be regarded as a medical treatment
institution within the meaning of this Law, it shall be a
stationary or mobile room equipped in conformity with the
services to be provided and suitable for the performance of
medical procedures. The procedures for establishing, deploying,
and equipping a temporary medical assistance point shall be
approved by the Commander of the National Armed Forces.
(2) A medical practitioner employed in a medical treatment
institution of the National Armed Forces shall carry out
professional activities outside the territory of Latvia in
accordance with the laws and regulations governing the field of
health care, unless otherwise specified in international
agreements binding on the Republic of Latvia. The fulfilment of
those requirements shall be controlled by the Joint Headquarters
of the National Armed Forces.
[18 June 2015]
Section 55.2 (1) Medical treatment
institutions may voluntarily join the jointly formed European
reference networks of health care providers and centres of
expertise in the Member States of the European Union the purpose
of which is to provide specialised high-quality health care for a
patient who has a rare, uncommon or complex disease.
(2) Requirements for medical treatment institutions wishing to
voluntarily join the European reference networks and the
procedures by which medical treatment institutions shall join
these networks shall be determined by the Cabinet.
[1 December 2016]
Section 56. (1) Certification of medical treatment
institutions and their structural units shall be voluntary.
(2) The Cabinet shall determine the procedures for certifying
medical treatment institutions and their structural units.
(3) A certificate for a medical treatment institution or its
structural units, in accordance with the health care financing
procedures stipulated by the Cabinet, shall give the relevant
medical treatment institution advantages when entering into a
contract with the National Health Service.
[1 June 2000; 10 December 2009; 21 June 2012]
Section 56.1 (1) If a medical treatment
institution provides assistance to a patient and there are
grounds for considering that the patient has suffered from
violence, the medical treatment institution shall notify the
State Police thereof without delay but not later than within 12
hours.
(2) If a medical treatment institution provides assistance to
an underaged patient and there are grounds for considering that
the patient has suffered from the lack of sufficient care and
supervision or other violation of the rights of the child, the
medical treatment institution shall notify the State Police
thereof without delay but not later than within 12 hours.
[7 October 2010]
Section 56.2 The head of a medical treatment
institution in the provision of health care shall, if necessary,
involve a medical treatment support person who has adequate
professional knowledge, as attested by an educational document
regarding the education acquired in the relevant profession.
[1 December 2016]
Section 57. The Cabinet shall determine the procedures
for the admission of residents and distribution thereof and for
financing residencies.
[1 June 2000; 1 December 2016]
Section 58.
[25 March 2004]
Section 59. The procedures for keeping medical
documents in medical treatment institutions shall be stipulated
by the Cabinet.
[25 March 2004; 27 May 2004; 10 December 2009]
Section 60. Regulations for the production of
prescription forms and procedures for writing out prescriptions
shall be governed by Cabinet regulations and other laws and
regulations.
Chapter X
Medical treatment of Alcohol, Narcotic, Psychotropic, Toxic
Substances, Gambling and Computer Game Addictive Illnesses
[27 May 2004]
Section 60.1 The Cabinet shall determine the
procedures for the examination of the effect of alcohol,
narcotic, psychotropic or toxic substances.
[27 May 2004]
Section 61. Medical treatment of alcohol, narcotic,
psychotropic, toxic substances, gambling or computer game
addiction shall be voluntarily if the addict wishes in addiction
treatment institutions in accordance with the procedures
stipulated by the Cabinet.
[27 May 2004]
Section 62. In cases where, as a result of the use of
alcohol, narcotic, psychotropic, toxic substances, participation
in gambling or computer games, a patient performs activities
dangerous to the public, systematically commits administrative
violations or by his or her actions endangers himself or herself,
his or her closest relatives or the public, the compulsory
measures of social and psychosocial rehabilitation prescribed by
law shall be applied, but for minors - compulsory measures of an
educational nature.
[1 June 2000; 27 May 2004]
Section 63. The compulsory measures for social and
psychosocial rehabilitation of alcohol, narcotic, psychotropic,
toxic substances, gambling or computer game addiction shall be as
follows:
1) registration in the police prophylactic register and a
warning in writing by the police that the patient must terminate
the use of alcohol, narcotic, psychotropic, toxic substances,
participation in gambling or computer games and the committing of
the related administrative violations, as well as to start
mandatory medical treatment;
2) registration in the register of addicts and development of
motivation to make the patient interested in undergoing voluntary
medical treatment for alcohol, narcotic, psychotropic, toxic
substances, gambling or computer game addiction;
3) a court ruling on the requirement for the convicted person
to undergo medical treatment.
[1 June 2000; 27 May 2004]
Section 64. In imposing a suspended sentence, a court
may impose, for a convicted person who has committed a crime
under the influence of alcohol, narcotic, psychotropic or toxic
substances, or is addicted to gambling or computer games, with
his or her consent the obligation to undergo treatment for
alcohol, narcotic, psychotropic, toxic substances, gambling or
computer game addiction at a social and psychiatric
rehabilitation institution.
[27 May 2004]
Chapter XI
Mental Illness
Section 65. Persons with mental disorders and mental
illness shall be ensured all the civil, political, economic, and
social rights provided for by law. Mental disorders or mental
illness shall not be a basis for discrimination of an
individual.
Section 66. Mentally ill persons have the right to
receive medical assistance and care of a quality that conforms
with accepted standards of general medicine.
Section 67. (1) Psychiatric assistance shall be based
upon the voluntary principle. In-patient assistance shall be
provided in a psychiatric medical treatment institution or a
medical treatment institution psychiatric department (hereinafter
- the psychiatric medical treatment institution) if due to the
state of health of the patient such assistance cannot be provided
on an out-patient basis or at the place of residence.
(2) A patient may be admitted to the psychiatric medical
treatment institution with his or her written permission on the
basis of a determined mental disorder and a justified decision by
a psychiatrist regarding the necessity for the investigation of
mental health, medical treatment, and rehabilitation in the
psychiatric medical treatment institution. The consent of the
patient for admission shall be appended to the medical
documents.
[1 March 2007; 10 December 2009]
Section 68. (1) Psychiatric assistance without the
consent of a patient shall be provided if the patient:
1) has threatened or threatens, tried or is trying to do
personal injuries to himself or herself or to another person or
has behaved or behaves violently to other persons and a medical
practitioner has determined that the patient has a mental health
disorder for which the possible consequences may be personal
injury to the patient himself or herself or another person;
2) the patient has indicated or indicates an inability to care
for himself or herself or for a person under his or her
guardianship and a medical practitioner has determined that the
patient has a mental health disorder for which the possible
consequences may be unavoidable and serious deterioration of the
person's health.
(2) In providing psychiatric assistance without the consent of
a patient in the cases specified in Paragraph one of this
Section, if it is possible, the necessity for providing
compulsory psychiatric assistance shall be explained to the
patient. The patient has the right to receive information on his
or her rights and obligations.
(3) If in providing psychiatric assistance it is necessary to
admit a patient to a psychiatric medical treatment institution
without his or her consent, a doctors' council of psychiatrists
shall, within a 72-hour period, examine the patient and take the
decision to provide psychiatric assistance in the psychiatric
medical treatment institution without his or her consent
(hereinafter - the decision to provide psychiatric assistance) or
to suspend such assistance.
(4) The doctors' council of psychiatrists shall, without
delay, notify the patient of its decision. If the doctors'
council of psychiatrists takes the decision to provide
psychiatric assistance, the lawful representative of the patient
shall be informed of this. If the patient does not have a lawful
representative, in respect of the decision taken, the doctors'
council of psychiatrists shall inform the spouse of the patient
or one of the nearest relatives of the patient (parents, adult
children, brothers or sisters), or, at the request of the
patient, another person. In deciding to which person the decision
to provide psychiatric assistance shall be notified, the point of
view of the patient shall be taken into account as far as
possible.
(5) If the doctors' council of psychiatrists has taken the
decision to provide psychiatric assistance, the psychiatric
medical treatment institution shall, not later than within 24
hours, inform in writing a district (city) court (in conformity
with the location of the psychiatric medical treatment
institution), sending it a true copy of the decision and copies
of the documents at the disposal of the psychiatric medical
treatment institution which justify the placement of the patient
in a psychiatric medical treatment institution as well as provide
information on the representative of the patient if there is
such.
(6) Upon receipt of the decision and the documents appended
thereto referred to in Paragraph five of this Section, the judge
shall, without delay, utilising accessible communication
resources (telephone, fax, electronic mail), as well as at the
same time sending the relevant notification by post, inform the
district (republic city) prosecutor (in conformity with the
location of the psychiatric medical treatment institution), the
representative of the patient and the psychiatric medical
treatment institution of the day, time, and place for the
examination of the submitted material.
(7) Upon determining that the patient does not have a
representative, the judge shall, after receipt of the documents
referred to in Paragraph six of this Section, immediately request
that the Latvian Council of Sworn Advocates assign a sworn
advocate for the representation of the interests of the patient
and at the same time inform the Latvian Council of Sworn
Advocates of the day, time, and place for the examination of the
submitted material.
(8) On the basis of a request from the prosecutor,
representative of the patient or advocate, the court shall ensure
the possibility to become acquainted with the decision and the
documents appended thereto referred to in Paragraph five of this
Section. On the basis of a request from the representative of the
patient or advocate, the psychiatric medical treatment
institution shall ensure the possibility to meet with the patient
in order to provide consultations.
(9) A judge shall examine the materials submitted regarding
the provision of psychiatric assistance in the psychiatric
medical treatment institution without the consent of the patient
in a closed sitting in the psychiatric medical treatment
institution in which the patient has been placed. The sitting
shall be attended by the patient (if his or her health condition
allows it), the prosecutor, representative of the patient or
advocate.
(10) The materials regarding the provision of psychiatric
assistance in the psychiatric medical treatment institution
without the consent of the patient shall be examined within a
period of 72 hours after receipt of the doctors' council of
psychiatrists decision. The judge on his or her own initiative or
also on the basis of a justified request from the prosecutor,
representative of the patient or advocate shall decide regarding
the deferral of examination of the materials for a period, which
is not longer than 48 hours if it is not possible to examine the
materials because one of the persons referred to in Paragraph
eight of this Section has not appeared or it is necessary to
acquire additional evidence. The decision of the judge cannot be
appealed, except for the decision in which a time is not
specified for the examination of the material.
(11) In examining the materials, the judge shall hear the
representative of the doctors' council of psychiatrists,
representative of the patient or advocate, the patient (if it is
possible), as well as the prosecutor and shall take the decision
to approve the decision of the doctors' council of psychiatrists
on the provision of psychiatric assistance for a period of up to
two months or to refuse to approve the decision of the doctors'
council of psychiatrists.
(12) In the examination of materials regarding the provision
of psychiatric assistance in the psychiatric medical treatment
institution without the consent of the patient, persons who are
involved in the medical treatment process of the patient are
permitted to attend. A judge may, on his or her own initiative or
also on the basis of a justified request from the prosecutor,
representative of the patient or advocate, hear also other
persons who may provide information on important circumstances in
the matter. The decision of the judge shall not be subject to
appeal.
(13) The decision of the judge to approve the decision of the
doctors' council of psychiatrists regarding the provision of
psychiatric assistance for a period of up to two months or
regarding a refusal to approve the decision of the doctors'
council of psychiatrists shall indicate the name of the relevant
court, the given name and surname of the judge, the date of the
examination of the materials, information on the psychiatric
medical treatment institution, on the persons who have
participated in the examination of the materials, and the
patient, reasons for the decision, the provisions of the law upon
which the judge based the decision, and the ruling, as well as
shall indicate the procedures for the appeal of the decision.
(14) The judge shall, without delay, notify the persons who
participated in the examination of the material of the decision.
A true copy of the decision shall be issued to the patient,
representative of the patient or advocate, as well as the
psychiatric medical treatment institution and the prosecutor. If
it is not possible to draw up the decision in writing without
delay (after the examination of materials regarding the provision
of psychiatric assistance without the consent of the patient), a
true copy thereof shall be sent to the persons referred to in the
first sentence of this Paragraph by post not later than the next
working day after notification of the decision. The decision
shall be implemented without delay.
(15) The persons referred to in Paragraph nine of this Section
as well as the patient may, within 10 days from the day of the
notification of the decision of the judge, submit an appeal to
the Court President but the prosecutor may submit a protest. The
written submitted appeal or protest shall be examined by the
Court President within 10 days from the end of the time period
for the submission of an appeal or protest. In examining an
appeal or protest, the Court President shall evaluate only the
arguments included in the appeal or protest.
(16) If the Court President, in examining the submitted appeal
or protest and the documents appended thereto, finds that the
decision of the judge is without justification, he or she shall
take the decision on the setting aside thereof. The decision of
the Court President shall, without delay, be notified to the
psychiatric medical treatment institution and the prosecutor as
well as to the submitter of the appeal. A true copy of the
decision shall be sent to the prosecutor, patient, representative
of the patient or advocate, as well as the psychiatric medical
treatment institution not later than on the next working day
after the day the decision was taken.
(17) Not later than seven days prior to the end of the time
period specified by the decision of the judge, the doctors'
council of psychiatrists shall repeatedly examine the patient and
take the decision on the necessity to continue to provide to the
patient psychiatric assistance in the psychiatric medical
treatment institution without his or her consent or on the
discontinuance of such assistance. If the doctor providing
medical treatment to the patient finds that the provision of
psychiatric assistance in the psychiatric medical treatment
institution is no longer necessary, the provision of psychiatric
assistance shall be suspended prior to the end of the time period
specified in the decision of the judge. If the doctors' council
of psychiatrists has taken the decision on the necessity to
continue to provide to the patient psychiatric assistance in the
psychiatric medical treatment institution without his or her
consent for a period of up to six months, the psychiatric medical
treatment institution shall perform the activities indicated in
Paragraph five of this Section. The doctors' council of
psychiatrists is entitled to take repeatedly the decision on the
necessity to continue to provide to the patient psychiatric
assistance in the psychiatric medical treatment institution
without his or her consent for another six months or on the
discontinuance of such assistance in conformity with the
procedures laid down in this Section.
(18) A judge shall examine the materials of the matter on the
further provision of psychiatric assistance to the patient in the
psychiatric medical treatment institution without his or her
consent or on the discontinuance of such assistance according to
the procedures specified in Paragraphs six to sixteen of this
Section and shall take the decision on the approval of the
doctors' council decision referred to in Paragraph seventeen of
this Section or on the refusal to approve the decision of the
doctors' council.
(19) The time periods for the provision of psychiatric
assistance without the consent of the patient shall be counted
from the moment when the patient, in the cases specified in
Paragraph one of this Section, has been conveyed to the
psychiatric medical treatment institution in order to receive
psychiatric assistance without his or her consent.
(20) A patient who is placed in a psychiatric medical
treatment institution for medical treatment in accordance with
the procedures laid down in this Section has the right, not more
than once in two months, to submit a submission to the district
(city) court (according to the location of a psychiatric medical
treatment institution) with a request to review the decision to
provide psychiatric assistance to the patient without his or her
consent.
[8 November 2007; 11 September 2014]
Section 68.1 (1) In the cases specified in
Section 68 of this Law, payment for the legal aid provided by the
advocate assigned by the Latvian Council of Sworn Advocates shall
be made as well as compensatory expenditures associated with the
provision of legal aid shall be reimbursed in conformity with the
laws and regulations which determine the amount of payment for
State ensured legal aid in civil cases, not taking into account
the restrictions specified therein in relation to the amount of
State ensured legal aid types. The Legal Aid Administration
shall, within a period of one month after receipt of the
notification submitted within the specified time period, make the
payment in accordance with the submitted notification of the
advocate regarding the legal aid provided from the State budget
funds intended for such purposes.
(2) The Legal Aid Administration shall make payments to an
advocate who has been assigned by the Latvian Council of Sworn
Advocates in the cases specified in Section 68 of this Law for
the following types of legal aid: for becoming acquainted with
the materials of the case, legal consultations, representation in
a court sitting in the psychiatric medical treatment institution,
as well as for the preparation of appeals to the Court
President.
(3) For the receipt of the payment, the advocate shall, within
two months, submit to the Legal Aid Administration an approved
notification regarding the provided legal aid.
(4) The notification regarding the provided legal aid, i.e.
becoming acquainted with the materials of the case,
representation in the court sitting in the psychiatric medical
treatment institution, and preparation of appeals to the Court
President, shall be approved by the judge or, in the case
specified in Section 68, Paragraph fifteen of this Law, by the
Court President. The notification shall indicate the given name
and surname of the advocate, personal identity number, address of
the practice, given name and surname of the patient, personal
identity number, the name of the court, the type of legal aid,
the date and time (number of hours) of the provision thereof, the
amount of payment (without value added tax), the name of the bank
and the account into which the payment shall be made, and
appending to it the documents which certify other compensatory
expenditures.
(5) The notification regarding the provided legal aid, i.e.
legal consultations provided to the patient, shall be approved by
an official of the psychiatric medical treatment institution. The
notification shall indicate the given name and surname of the
advocate, personal identity number, address of the practice,
given name and surname of the patient, personal identity number,
the number of the material, the type of legal aid, the date and
time (number of hours) of the provision thereof, the amount of
payment (without value added tax), the name of the bank and the
account into which the payment shall be made, and appending to it
the documents which certify other compensatory expenditures.
[8 November 2007]
Section 69. (1) If a person disturbs public order due
to a mental disorder or mental disease, his or her detention,
conveyance to and supervision at the psychiatrist shall be
performed by police officers in accordance with the law On
Police.
(2) The police officers shall submit to the psychiatrist a
notice in writing of the anti-social nature of the behaviour of
the patient.
Section 69.1 (1) A patient who is admitted
in a psychiatric medical treatment institution without his or her
consent, a patient who has been taken to an inpatient medical
treatment institution for the performance of psychiatric
examination until a court decision, and a patient for whom
medical treatment in the psychiatric medical treatment
institution has been determined as a compulsory measure of
medical nature in criminal proceedings has:
1) the rights and obligations of a patient laid down in the
Law on the Rights of Patients;
2) the right to receive and send letters, to receive postal
items (parcels), to use communication means in order to get in
touch with persons outside a psychiatric medical treatment
institution, to meet with relatives and other persons, and also
the right to a daily walk.
A medical practitioner shall immediately inform a patient of
such rights in the form understandable for him or her and taking
into account the age, maturity, and experience of the patient. If
necessary, the medical practitioner shall repeatedly provide the
abovementioned information.
(2) If there are direct threats that a patient, due to mental
disorders, may commit injuries to himself or herself or other
persons, or a patient demonstrates violence towards other
persons, a doctor has the right to prohibit the patient's meeting
with relatives and other persons and a daily walk. The
prohibition shall be immediately cancelled if the threat caused
by the patient does not exist anymore. The doctor shall indicate
the reason and duration of application of the prohibition in the
medical documentation of the patient.
(3) The Cabinet shall determine the list of those items which
are prohibited to be kept in a psychiatric medical treatment
institution and to receive in consignments (parcels).
(4) A doctor, having assessed each case, may take the decision
regarding a patient's meeting with relatives and other persons at
the presence of a medical practitioner if it is necessary due to
safety considerations or it is requested by a visitor or patient.
A doctor shall indicate the decision taken and substantiation
thereof in the medical documentation of the patient.
(5) If a medical practitioner has justified doubts that items
prohibited in a medical treatment institution are kept by a
patient or present in his or her belongings, a doctor has the
right to take the decision regarding searching of the patient or
his or her belongings. A doctor shall indicate the decision taken
and substantiation thereof in the medical documentation of the
patient. A medical treatment institution shall ensure that
searching of the patient is carried out by a medical practitioner
of the same gender.
(6) In cases when there are direct threats that a patient, due
to mental disorders, may commit injuries to himself or herself or
other persons or a patient demonstrates violence towards other
persons and attempts to discontinue threat by verbal convincing
have failed, the following confining means may be used in
psychiatric medical treatment institutions:
1) physical confinement by using physical force for
confinement of movements of the patient;
2) mechanical confinement by using confining cords or
belts;
3) injection of medicines to a patient against his or her
will;
4) placement in a monitoring ward.
(7) Confining means may be used for a patient by force only in
such case if the patient is hospitalised in a psychiatric medical
treatment institution without his or her consent, taken to an
inpatient medical treatment institution for conducting a
psychiatric examination or for a patient for whom medical
treatment in a psychiatric medical treatment institution has been
determined as a compulsory measure of medical nature. Confining
means, in conformity with the conditions referred to in this
Section, may be applied also in the case when psychiatric
assistance is provided to a patient without his or her consent
before the decision of the judge referred to in Section 68,
Paragraph eleven of this Law is taken.
(8) The decision to apply confining means shall be taken by a
doctor and implemented by a medical practitioner. Application of
confining means shall be proportional to the direct threat caused
by a patient and application thereof shall be immediately
discontinued if the threat caused by the patient does not exist
anymore. A doctor shall indicate application of confining means
in the medical documentation of a patient by indicating the
reasons for application of confining means, the starting and end
time and injuries caused, if any have been caused for the patient
or medical practitioner.
(9) The Cabinet shall determine unified internal procedure
standards for such psychiatric medical treatment institutions or
their units in which the patients referred to in Paragraph one of
this Section have been placed, including the procedures for the
searching of patients and the consignments (parcels) addressed to
them, and also the procedures for the carrying out of confining
of patients, also using confining means.
(10) A patient has the right to appeal the decisions referred
to in Paragraphs two and six of this Section within one month to
the head of the medical treatment institution who shall examine a
submission and take the decision within seven days. A patient has
the right to appeal the decision of the head of the medical
treatment institution to the Health Inspectorate within one month
which shall examine a submission and take the decision within 20
days. A patient has the right to appeal the decision of the
Health Inspectorate to the district (city) court within one
month. A judgment of the district (city) court may not be
appealed.
[11 September 2014; 6 December 2023]
Section 69.2 A person for whom a compulsory
measure of medical nature has been determined in criminal
proceedings shall, within 14 days after receipt of the true copy
of the court decision, contact the medical treatment institution
indicated in the court decision in person or remotely in order to
agree on the commencement of medical treatment, except for a
person who, according to the court decision, is taken to the
medical treatment institution under escort of a police
employee.
[6 December 2023]
Section 69.3 (1) A person for whom a
compulsory measure of medical nature has been determined in
criminal proceedings shall undergo medical treatment in the
medical treatment institution indicated in the court decision.
Medical treatment in another medical treatment institution may be
commenced only according to a new court decision.
(2) A submission to the court with a justification for
changing the medical treatment institution shall be submitted by
the person for whom medical treatment in a psychiatric medical
treatment institution has been determined as a compulsory measure
of medical nature in criminal proceedings, by the representative
of such person, or by the medical treatment institution in which
the abovementioned person is undergoing medical treatment
according to the court decision.
(3) The medical treatment institution which takes over medical
treatment of such person for whom a compulsory measure of medical
nature has been determined in criminal proceedings has the right
to receive complete information on the medical treatment
previously ensured to such person and on the results thereof.
Information shall be provided in accordance with the laws and
regulations governing personal data protection and also the laws
and regulations regarding keeping of medical documents.
[6 December 2023]
Section 70.
[1 March 2007]
Section 70.1 (1) A medical practitioner
shall, without delay, inform the court which took the decision on
the determination of a compulsory measure of medical nature
if:
1) the person for whom such compulsory measure was determined
in criminal proceedings is evading it or does not fulfil the
corresponding conditions;
2) the health condition of the person no longer corresponds to
the determined compulsory measure of medical nature.
(2) The content and amount of information to be provided to
the court shall be determined by the Cabinet.
[1 December 2016; 6 December 2023]
Chapter XII
Health and Ability to Work, Forensic and Legal Psychiatric
Examination
Section 71. In cases of persistent or permanent
restrictions of physical or mental capacity and in cases of
functional restrictions of the body, at the activity and
participation level, health and work disability examination shall
be performed and disability shall be determined by the Medical
Commission for Expert-Examination of Health and Working Ability
(MCEEHWA) authorised by the State, the operation of which shall
be governed by laws and regulations.
[8 June 2006 / See Transitional Provisions]
Section 72. Court forensic and court psychiatric
examination shall be performed in accordance with the decision
taken by the institution (official), investigator, participant of
an investigation group, prosecutor or the court (judge) in
accordance with the procedures laid down in law. The Cabinet
shall determine the procedures for the performance of court
forensic and court psychiatric examination.
[16 June 2010]
Section 73.
[1 June 2000]
Chapter XIII
Suspension of the Operations of a Medical Treatment Institution
of the Structural Unit Thereof or Suspension of Health Care
Service Provided Thereby
[8 May 2008; 11 September
2014]
Section 74. The decision to suspend the operations of a
medical treatment institution or the structural unit thereof or
to suspend the health care service provided thereby if the laws
and regulations governing the field of medical treatment have
been infringed shall be taken by the manager of the Health
Inspectorate and his or her deputies, or by the manager of the
territorial office of the Health Inspectorate and his or her
deputies.
[11 September 2014]
Section 75. (1) If the Health Inspectorate inspector
has determined such a violation of the laws and regulations
governing the field of medical treatment which create a risk for
the course of a successful medical treatment process, he or she
shall express a written warning to the medical treatment
institution. All the determined violations of the laws and
regulations governing the field of medical treatment shall be
indicated in the warning and recommendations shall be provided,
as well as the time period for the rectification of the
violations shall be determined.
(2) Taking into account the impact of the violation on the
medical treatment process and the actual possibilities of the
rectification thereof, the time period for the rectification of
the violation included in the warning shall be not shorter
than:
1) two years if for the rectification of the violation capital
construction is necessary;
2) six months if for the rectification of the violation
partial reconstruction of a building or capital repairs of
equipment is necessary.
(3) In the rest of the cases which are not referred to in
Paragraph two of this Section, the Health Inspectorate inspector,
taking into account the impact of the violation on the medical
treatment process and the actual possibilities of the
rectification thereof, shall determine a time period for the
rectification of the violation from one month to six months.
(4) If the infringements indicated in the warning are not
rectified in the specified time period, the officials referred to
in Section 74 of this Law shall take the decision to suspend the
operations of the relevant medical treatment institution or the
structural unit thereof or to suspend the health care service
provided thereby.
(5) The suspension of the operation of medical treatment
institutions or the structural unit thereof shall be ensured by
the head of the medical treatment institution with the
participation of the official who took the decision to suspend
the operations of the medical treatment institution or the
structural unit thereof, or his or her authorised official.
Suspension of the health care service provided by the medical
treatment institution shall be ensured by the head of the medical
treatment institution.
(6) The suspension of the operation of a medical treatment
institution or the structural unit thereof or the suspension of
the provided health care service shall be performed so that:
1) the determined violations may be rectified without
hindrance;
2) the damage to premises and equipment due to meteorological
conditions or corrosion is reduced as far as possible;
3) the operations of other structural units and equipment is
disturbed as little as possible.
(7) Control of the suspension of the operation of a medical
treatment institution or the structural unit thereof or control
of the suspension of the provided health care service shall be
ensured by an official who has taken the decision to suspend the
operation or to suspend the health care service, or his or her
authorised person.
(8) The operation of a medical treatment institution or the
structural unit thereof or the provided health care service may
be suspended without previous warning if, due to infringements of
the laws and regulations governing the field of medical
treatment, a threat is created to human health and life.
(9) The official who has the right to take the decision
referred to in Paragraph eight of this Section shall take it
within three working days after it became known to him or her
regarding the infringements of the laws and regulations governing
the field of medical treatment referred to in Paragraph eight of
this Section, and it is to be implemented without delay.
[11 September 2014]
Section 76. (1) The relevant medical treatment
institution shall notify in writing the official who has taken
the decision to suspend the operation of a medical treatment
institution or to suspend the operation of the structural unit
thereof or to suspend the health care service provided thereby
regarding rectification of the infringements of the laws and
regulations governing the field of medical treatment. Such
official shall, within five working days after receipt of the
notification, verify whether the relevant violations have been
rectified.
(2) If all infringements referred to in a written warning or
decision to suspend operation of the medical treatment
institution or structural unit thereof, or to suspend the
provided health care service, have been rectified, the relevant
official shall, within three working days after performance of
the inspection, issue a written permission to renew operation of
the medical treatment institution or structural unit thereof, or
provision of health care service.
(3) If all infringements referred to in a written warning or
decision to suspend operation of the medical treatment
institution or structural unit thereof, or to suspend the
provided health care service, have not been rectified, the
relevant official shall, within three working days after
performance of the inspection, notify of the refusal to issue a
permission to renew operation of the medical treatment
institution or structural unit thereof, or provision of health
care service.
[11 September 2014]
Section 77. (1) A submission where the decision of the
Health Inspectorate to suspend operation of the medical treatment
institution or structural unit thereof, or to suspend the
provided health care service without prior warning is contested
shall be examined and the decision shall be taken within 10
working days after receipt of the submission.
(2) The contesting and appeal of the decisions referred to in
this Section shall not suspend the fulfilment thereof.
[11 September 2014]
Chapter XIV
Health Information System
[7 October 2010]
Section 78. (1) In order to ensure organisation of
health care and to facilitate the provision of health care
services, the data of the health sector shall be accumulated in
the health information system.
(2) The Cabinet shall determine the manager of the health
information system, the data to be stored in the health
information system and the procedures for processing them, as
well as the procedures for issuing data.
(3) [22 November 2017]
[22 November 2017]
Section 79. (1) In order to ensure accumulation of true
and current information and completeness of information in the
health information system, the manager or holder of such system,
if the functions of the holder of the health information system
have been transferred to an authorised institution, is entitled
to request and receive free of charge information from State and
local government institutions, medical treatment institutions,
medical practitioners, and patients.
(11) Inclusion of data in the health information
system shall be making of an entry or completing of a structured
electronic document in the online regimen. The entry shall be
certified with a safe electronic signature or other system
authentication tools and procedures which ensure authenticity of
the entry and approve the identity of the signatory. The
procedures for the use of system authentication tools and also
the procedures for ensuring the authenticity of procedural
entries shall be determined by the Cabinet.
(12) Records made or documents created in the
health information system shall have legal force even if they do
not contain the detail "signature" (not signed with a secure
electronic signature with a time stamp or an electronic
signature).
(2) The information accumulated in the health information
system regarding patients shall be provided in accordance with
the Law on the Rights of Patients. Other information shall be
provided free of charge in accordance with the procedures laid
down in laws and regulations:
1) to medical treatment institutions, medical practitioners,
medical support persons according to their competence;
2) to employees of a medical treatment institution (for
example, an employee of the reception at a medical treatment
institution) according to carrying out the official duties;
3) to undertakings manufacturing medicinal products, drug
wholesalers, pharmacies, pharmacists and pharmacist's assistances
according to their competence.
(3) Information regarding electronic sick-leave certificates
in conformity with the laws and regulations regarding the health
information system shall be transmitted to the information
systems of the State Revenue Service, thereby providing the
employer with the information on the electronic sick-leave
certificate issued to the employee for three years from the time
of receipt thereof in the information systems of the State
Revenue Service.
[11 September 2014; 1 December 2016]
Section 80. The manager or holder of the health
information system, if the functions of the holder of such system
have been transferred to an authorised institution, is entitled
not to inform the data subject of the processing of personal data
in the health information system, unless the data subject is
specifically requesting it and processing of personal data is
necessary for:
1) the needs of medical treatment;
2) the provision of health care services or their
administration;
3) the distribution of medicinal products and medical devices
or their administration;
4) the collection of statistical information specified by the
State.
Chapter XV
Special Provisions of Economic Activity of a Medical Treatment
Institution
[11 September 2014]
Section 81. (1) If delay is related to agreements on
delivery of goods, purchase or provision of a service and a
debtor is a medical treatment institution which conforms to the
criteria of a commissioning party in accordance with the laws and
regulations in the field of public procurements or criteria of a
public institution in accordance with the laws and regulations in
the field of providers of public services (a public commissioning
party), the provisions of the Civil Law which are applicable to
agreements on delivery of goods, purchase or provision of a
service shall be applied to the delay, taking into account the
time period of delay of the debtor laid down in Paragraph two of
this Section.
(2) If a medical treatment institution has not made the
payment in the cases abovementioned in Paragraph one of this
Section within 60 days after the setting in of the conditions
referred to in Section 1668.2, Paragraph one of the
Civil Law, the delay shall set in with all consequences arising
therefrom.
[See Paragraph 21 of Transitional Provisions]
Chapter XVI
Administrative Offences in the Field of the Provision of Health
Care Services and Competence in Administrative Offence
Proceedings
[21 May 2020 / Chapter shall
come into force on 1 July 2020. See Paragraph 33 of Transitional
Provisions]
Section 82. For practising medicine without medical
education, a fine from ten to seventy units of fine shall be
imposed.
[21 May 2020 / This Section shall come into force on 1 July
2020. See Paragraph 33 of Transitional Provisions]
Section 83. For practising medicine without
registration in accordance with the procedures specified in laws
and regulations, a fine from two to twenty-eight units of fine
shall be imposed on a natural person but a fine from fifty to two
hundred and fifty units of fine on a legal person.
[21 May 2020 / This Section shall come into force on 1 July
2020. See Paragraph 33 of Transitional Provisions]
Section 84. For violations of providing medical
opinions or violations of health care, a warning or a fine of up
to one hundred units of fine shall be imposed on a natural
person, removing the right to practice medicine for a period of
six months to two years or without this, but a fine from fifty to
five hundred and fifty units of fine on a legal person.
[21 May 2020 / This Section shall come into force on 1 July
2020. See Paragraph 33 of Transitional Provisions]
Section 85. For violations of the use of medical
devices in a medical treatment institution, a fine from ten to
seventy units of fine shall be imposed on a natural person but a
fine from fifty to two hundred and fifty units of fine on a legal
person.
[21 May 2020 / This Section shall come into force on 1 July
2020. See Paragraph 33 of Transitional Provisions]
Section 85.1 For the violations of the
procedures for conducting clinical trials of medical devices
intended for human use or performance studies on in vitro
diagnostic medical devices, a warning or a fine from five to
forty units of fine shall be imposed on a natural person but a
fine from fifty to four hundred units of fine on a legal
person.
[6 December 2023]
Section 86. For non-compliance with the regulations for
the keeping of prescription forms or procedures for issuing
prescriptions, a fine from seven to seventy units of fine shall
be imposed on a natural person but a fine from fifty-six to two
hundred and eighty units of fine on a legal person.
[21 May 2020 / This Section shall come into force on 1 July
2020. See Paragraph 33 of Transitional Provisions]
Section 87. For non-compliance with the procedures for
the issuance and cancellation of a sick-leave certificate, a fine
from twenty-eight to two hundred and eighty units of fine shall
be imposed.
[21 May 2020 / This Section shall come into force on 1 July
2020. See Paragraph 33 of Transitional Provisions]
Section 88. Administrative offence proceedings for the
offences referred to in Sections 82, 83, 84, 85, 85.1,
86, and 87 of this Law shall be conducted by the Health
Inspectorate.
[21 May 2020; 6 December 2023]
Transitional Provisions
1. Medical practitioners who have acquired a qualification
category or a certificate in any of the sub-specialities or
additional specialities and have practised it for more than five
years may continue his or her practice without obtaining a
primary speciality certificate. Certification of such specialists
shall take place in the acquired sub-speciality or additional
speciality.
2. Medical practitioners who have acquired a qualification
category or a certificate in any of the primary specialities,
sub-specialities or additional specialities and have practised it
for more than ten years, upon a change in the classification of
specialities, may continue his or her practice without obtaining
a primary speciality certificate if such speciality is recognised
as a medical treatment or diagnostic method.
3. [1 June 2000]
4. With the coming into force of this Law, Cabinet Regulation
No. 177, Regarding Medical Treatment, issued in accordance with
Article 81 of the Constitution (Latvijas Republikas Saeimas un
Ministru Kabineta Ziņotājs, 1994, No. 19; 1995, No. 4; and
1997, No. 5), is repealed.
5. Medical treatment institutions and their structural units
which were established before 30 June 2000 shall be evaluated by
31 December 2001 in conformity with the mandatory
requirements.
[1 June 2000]
6. The Cabinet shall, by 1 November 2004, issue the
regulations referred to in Section 4, Section 9, Paragraph one,
Section 17, Paragraph one (wording of 27 May 2004), Sections 59
and 60.1 of this Law.
[27 May 2004; 16 June 2005; 8 June 2006]
7. The Cabinet shall, by 1 October 2005, issue the regulations
referred to in Section 9, Paragraph two and Section 34, Paragraph
three in the wording of 16 June 2005 of this Law.
[16 June 2005; 8 May 2008]
8. The Cabinet shall, by 1 January 2007, issue the regulations
referred to in Section 9.1, Paragraph two and Section
33 in the wording of 8 June 2006 of this Law.
[8 June 2006; 8 May 2008]
9. Amendments to Section 4, Paragraph two, the new wording of
Section 27 and the new wording of Section 37, Paragraph two of
this Law shall come into force on 1 January 2007.
[8 June 2006]
10. The new wording of Section 37, Paragraph one, Clause 2 of
this Law shall come into force on 1 July 2009. Up to 30 June
2009, a doctor shall, within the scope of his or her professional
activities, evaluate illnesses and the consequences caused
thereof.
[8 June 2006]
11. The new wording of Section 71 of this Law shall come into
force on 1 July 2009.
[8 June 2006]
12. In order to receive payment for the representation of a
patient which was performed up to 31 December 2007, advocates
assigned by the Latvian Council of Sworn Advocates shall, by 1
March 2008, submit to the Legal Aid Administration completed
notifications according to the procedures specified in Section
68.1, Paragraphs four and five of this Law, and
appending to them documents which certify other compensatory
expenditures.
[8 November 2007]
13. The new wording of Section 17, Paragraph three of this Law
shall come into force on 1 July 2008.
[8 May 2008]
14. The new wording of Section 26, Paragraphs one and two,
Section 29, Paragraphs two and three, and Section 33, Paragraph
three of this Law shall come into force on 1 January 2009.
[8 May 2008]
15. Section 29, Paragraph five of this Law shall come into
force on 1 January 2010.
[8 April 2009]
16. The amendment to Section 50 of this Law in relation to the
Health Payment Centre and the amendment regarding the deletion of
Section 52 shall come into force on 1 October 2009.
[18 June 2009]
17. [1 December 2016]
18. The Cabinet shall, by 1 December 2013, issue the
regulations referred to in Section 53.2, Paragraph
four of this Law. Until the day of coming into force of the
abovementioned Cabinet regulations, an opinion on whether a
person has lost the ability to understand the meaning of his or
her actions and to control them due to mental or health disorders
shall be provided by a commission established by the head of the
medical treatment institution in the composition of at least
three doctors one of whom is a psychiatrist. The costs of the
opinion and the statements issued on the basis thereof shall be
covered according to the price list of paid services of the
medical treatment institution:
1) by the future authorised person who requested the statement
on the basis of Section 53.2, Paragraph two, Clause 1
of this Law;
2) by the Court Administration within one month after request
of the medical treatment institution on the basis of Section
53.2, Paragraph two, Clause 2 of this Law.
[18 April 2013]
19. The Cabinet shall, by 1 December 2014, issue the
regulations referred to in Section 69.1, Paragraph
three of this Law.
[11 September 2014]
20. The Cabinet shall, by 1 January 2015, issue the
regulations referred to in Section 69.1, Paragraph
nine of this Law. Until the day of coming into force of the
abovementioned Cabinet regulations, the confinement of patients
by using confining means shall be carried out in conformity with
the medical technologies approved in accordance with the laid
down procedures.
[11 September 2014]
21. Provisions of Section 81 of this Law shall not be
applicable to the agreements entered into until the day of coming
into force of Section 81 of this Law and to the agreements that
have been entered into in accordance with the laws and
regulations in the field of granting of public procurements or
concessions after the day of coming into force of Section 81, if
procurements or concession procedures in accordance with the
procedures laid down in the laws and regulations have been
commenced until the day of coming into force of Section 81 of
this Law.
[11 September 2014]
22. The amendment to Section 45.1, Paragraph one of
this Law regarding the deletion of the word "riding therapist"
shall come into force on 1 January 2018.
[1 December 2016]
23. The amendment to Section 45.1, Paragraph one of
this Law regarding the addition of the word "optometrist" thereto
shall come into force on 1 January 2020.
[1 December 2016]
24. Section 54.1, Paragraph two of this Law shall
come into force on 1 January 2020.
[1 December 2016]
25. The Cabinet shall, by 1 April 2017, issue the regulations
referred to in Section 70.1, Paragraph two of this
Law.
[1 December 2016]
26. The Cabinet shall draw up and submit amendments to the
Medical Treatment Law to the Saeima in the package of the
draft State budget law for 2018 which provides for a gradual
withdrawal from the extended normal working time referred to in
Section 53.1 of this Law for medical practitioners and
persons of the team of emergency medical assistance who are not
medical practitioners, ensuring access to medical treatment.
[8 June 2017]
27. Until the date of the coming into force of the law
referred to in Paragraph 26 of the Transitional Provisions for
the medical practitioners and persons of the team of emergency
medical assistance who are not medical practitioners:
1) an extended normal working time may be specified which
shall not exceed 55 hours a week;
2) in the case of an extended normal working time, the work
remuneration for a working time which exceeds the normal working
time specified in the Labour Law shall be determined in
proportion to the increase in working time in the amount of not
less than 1.10 hourly wages specified.
[8 June 2017]
28. In order to ensure the fulfilment of the requirements of
Section 53.1 of this Law and Paragraph 27 of the
Transitional Provisions, the additional expenditure
necessary:
1) for 2017 shall be covered by programme 02.00.00 "Funds for
Unforeseen Events" of the State budget unit 74 "Funding to be
Reallocated in the Process of Implementation of the Annual State
Budget";
2) for 2018 and subsequent years shall be incorporated by the
Cabinet into the base expenditure budget of the Ministry of
Health.
[8 June 2017]
29. Section 53.1 of this Law is repealed on 1
January 2022.
[20 December 2018]
30. In order to ensure access to medical treatment, medical
practitioners and persons of the team of emergency medical
assistance who are not medical practitioners:
1) from 1 January 2018 to 31 December 2018 may be prescribed
an extended normal working time which shall not exceed 50 hours a
week;
2) [20 December 2018].
[22 November 2017; 20 December 2018]
31. [Declared null and void from 1 January 2019 by the
judgment of the Constitutional Court of 15 May 2018]
32. The amendment to Section 4 of this Law regarding the
deletion of Paragraph one and the amendment regarding the
deletion of Chapter IV shall come into force simultaneously with
the coming into force of the Health Care Financing Law.
[22 November 2017]
33. Section 10.1 and Chapter XVI of this Law shall
come into force simultaneously with the Law on Administrative
Liability.
[21 May 2020]
34. The Cabinet shall, by 31 December 2022, issue the
regulations referred to in Section 34, Paragraph two, Clauses 1,
2, 3, 4, and 5 of this Regulation. Until the day of coming into
force of the abovementioned Cabinet regulations, Cabinet
Regulation No. 689 of 28 November 2017, Procedures for the
Registration, Conformity Assessment, Distribution, Operation and
Technical Supervision of Medical Devices, and Cabinet Regulation
No. 891 of 21 September 2010, Procedures for the Clinical Trial
of Medical Devices Intended for Human Use, shall be applicable,
insofar as they are not in contradiction with this Law.
[13 January 2022]
35. A nurse who has not obtained an educational document
certifying that the specific speciality of a nurse or the
relevant medical treatment or diagnostic method has been acquired
in practice as a nurse but who, on 24 January 2022, held a valid
certificate of a medical practitioner in the specific speciality
of a nurse or the relevant medical treatment or diagnostic method
in practice as a nurse may continue to independently engage in
medical treatment in the specific speciality of a nurse and the
relevant medical treatment or diagnostic method in practice as a
nurse.
[13 January 2022]
36. Section 9.2 of this Law shall come into force
on 1 January 2024.
[21 April 2022]
37. Section 9, Paragraph 3.1 of this Law shall come
into force on 2 January 2024.
[6 December 2023]
38. Section 1, Clause 34 and Section 9, Paragraph six of this
Law shall come into force on 1 April 2024.
[6 December 2023]
39. The Cabinet shall, by 1 June 2024, issue the Cabinet
regulations referred to in Section 69.1, Paragraph
nine of this Law. Until the day of coming into force of these
regulations, Cabinet Regulation No. 453 of 12 July 2016,
Regulations Regarding the Procedures for Confining Patients and
the Objects Prohibited to be Kept in a Psychiatric Medical
Treatment Institution, shall be applicable insofar as it is not
in contradiction with this Law.
[6 December 2023]
40. Amendment to Section 9, Paragraph one of this Law
regarding the deletion of the words "medical practitioners,
medical treatment support persons" and also amendment regarding
the supplementation of this Section with Paragraph 1.1
shall come into force on 1 October 2024.
[6 December 2023 / The abovementioned amendments
shall be included in the wording of the law as of 1 October
2024]
41. The Cabinet shall, by 1 October 2024, issue the Cabinet
regulations referred to in Section 29, Paragraph one of this Law.
Until the day of coming into force of these regulations, Cabinet
Regulation No. 943 of 18 December 2012, Procedures for
Certification of Medical Practitioners, shall be applicable
insofar as it is not in contradiction with this Law.
[6 December 2023]
42. The new wording of Section 33, Paragraph three of this Law
shall come into force on 1 October 2024.
[6 December 2023 / The abovementioned amendment
shall be included in the wording of the law as of 1 October
2024]
43. Section 1, Clauses 32, 33, and 35, Section 9, Paragraph
seven, and Section 10.2 of this Law shall come into
force on 1 July 2025.
[6 December 2023 / The abovementioned amendments
shall be included in the wording of the law as of 1 July
2025]
44. The Cabinet shall, by 1 July 2025, issue the Cabinet
regulations referred to in Section 9.1, Paragraph two
of this Law. Until the day of coming into force of these
regulations, Cabinet Regulation No. 469 of 25 May 2010,
Procedures for the Development, Evaluation, Registration and
Implementation of Clinical Guidelines, shall be applicable
insofar as it is not in contradiction with this Law.
[6 December 2023]
Informative Reference to the
European Union Directives
[8 June 2006; 8 April 2009; 11
September 2014]
This Law contains legal norms arising from:
1) Council Directive 93/42/EEC of 14 June 1993 concerning
medical devices;
2) Council Directive 2004/83/EC of 29 April 2004 on minimum
standards for the qualification and status of third country
nationals or stateless persons as refugees or as persons who
otherwise need international protection and the content of the
protection granted;
3) Directive 2004/38/EC of the European Parliament and of the
Council of 29 April 2004 on the right of citizens of the Union
and their family members to move and reside freely within the
territory of the Member States amending Regulation (EEC) No
1612/68 and repealing Directives 64/221/EEC, 68/360/EEC,
72/194/EEC, 73/148/EEC, 75/34/EEC, 75/35/EEC, 90/364/EEC,
90/365/EEC and 93/96/EEC (Text with EEA relevance);
4) Directive 2003/88/EC of the European Parliament and of the
Council of 4 November 2003 concerning certain aspects of the
organisation of working time;
5) Directive 2007/47/EC of the European Parliament and of the
Council of 5 September 2007 amending Council Directive 90/385/EEC
on the approximation of the laws of the Member States relating to
active implantable medical devices, Council Directive 93/42/EEC
concerning medical devices and Directive 98/8/EC concerning the
placing of biocidal products on the market;
6) Directive 2011/7/EU of the European Parliament and of the
Council of 16 February 2011 on combating late payment in
commercial transactions;
7) Directive 2011/24/EU of the European Parliament and of the
Council of 9 March 2011 on the application of patients' rights in
cross-border healthcare.
The Law shall come into force on 1 October 1997.
The Law has been adopted by the Saeima on 12 June
1997.
President G. Ulmanis
Rīga, 1 July 1997
1 The Parliament of the Republic of
Latvia
Translation © 2024 Valsts valodas centrs (State
Language Centre)