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Republic of Lithuania Law on the Control of Narcotic and Psychotropic Substances

Įstatymas VIII-602 1998.01.08
1998.01.08 Išvertė: Lietuvos Respublikos Seimo kanceliarija Dokumentų skyrius .
1998.01.08 Teisės aktą priėmė: Lietuvos Respublikos Seimas .
Susiję dokumentai Originalus Microsoft Word 97 formato tekstas
 
                                           Official Translation 
 
REPUBLIC OF LITHUANIA
REPUBLIC OF LITHUANIA LAW ON THE CONTROL OF NARCOTIC AND PSYCHOTROPIC SUBSTANCES 
January 8, 1998. No. VIII-602
Vilnius 
CHAPTER ONE 
GENERAL PROVISIONS 
       ARTICLE 1. Objective of the Law 
       This Law shall establish the principles of the classification of narcotic and psychotropic substances, for lawful circulation of these substances when they are used for health care, veterinary and scientific purposes and circulation control, in accordance with the requirements of international agreements. 
       ARTICLE 2. The Basic Definitions in This Law  
       1. Narcotic and Psychotropic Substances means the biological and synthetic substances included in the lists of controlled substances, approved by the Ministry of Health, the harmful effects or misuse whereof, give rise to serious deterioration of human health, marked by mental and physical dependence on them, or pose danger to human health.
       2. Preparation means a drug 
product of any physical form, which has been accorded a certain drug form 
included in which can be found therapeutic doses of one or more narcotic or 
psychotropic drug substances.
       3. Lawful circulation 
production, processing, acquisition, wholesale or retail trade, keeping, 
internal transportation, import or export of narcotic or psychotropic substances 
in seeking to utilise these for health care, veterinary, law protection, science 
and science instruction purposes without violating any laws, and requirements of 
other legal acts.
       4. License (permit) means a 
document, issued according to the procedure established by the Government of the 
Republic of Lithuania and granting the right to acquire, keep, transport 
internally within the state, manufacture, process, import and export and also, 
use in wholesale or retail trade.
       5. Import means the bringing 
in of narcotic and psychotropic substances into the customs area of the Republic 
of Lithuania.
       6. Export means the 
transporting out of the customs area of the Republic of Lithuania of narcotic 
and psychotropic substances. 
       7. Transit means the 
transporting of narcotic and psychotropic substances across the customs 
territory of the Republic of Lithuania under, customs supervision.. 
 
             ARTICLE 3. The Names of Narcotic and Psychotropic Substances 
       Narcotic and psychotropic substances shall be included in the lists of controlled substances, approved by the Ministry of Health, under their international names, and in the absence thereof, under their chemical names. Included also, may be another common use name, which is more familiar to users.  
       ARTICLE 4. The Principles in 
Classification of Narcotic and      Psychotropic 
Substances 
       1. Narcotic and psychotropic 
substances shall be classified according to their harmful effect upon human 
health, when they are being misused, and according to whether they can be used 
for health care purposes. Based upon Republic of Lithuania international 
agreements, the Ministry of Health shall classify and include narcotic and 
psychotropic substances in the lists according to the control regimen applied to 
them.
       2. Three lists of narcotic and psychotropic substances shall be compiled:
       1) the first list shall be comprised of plants, narcotic and psychotropic substances the use whereof is prohibited in health care, because they bring about harmful consequences to human health, when they are being misused (further - List I);
       2) the second list shall be 
comprised of plants, narcotic and psychotropic substances, used for health care 
purposes, which are very dangerous to human health due to the harmful 
consequences arising when these substances are being misused (further - List 
II);
       3) the third list shall be 
comprised of plants and psychotropic substances used for health care purposes, 
which are dangerous to human health due to the harmful consequences of the 
misuse of these substances. (further - List III).  
       ARTICLE 5. The Classification of Preparations 
       Preparations shall be classified according to the narcotic and psychotropic substances present in them. Preparations shall be applied the control regimen of the substances present in them. If different control regimens are applied to substances present there, the preparation shall be applied that control regimen, which corresponds to the strictest control regimen applied to a substance within its composition.  
       ARTICLE 6. Advertisement of Narcotic and Psychotropic Substances 
       1. Advertisement of narcotic and psychotropic substances shall be prohibited.
       2. Information regarding 
drugs that are narcotic and psychotropic substances shall be provided to health 
care, pharmaceutical and veterinary specialists and consumers, according to the 
procedure established by the Ministry of Health. 
CHAPTER TWO 
THE REQUIREMENTS OF ACTIVITY INVOLVING THE SUBSTANCES INCLUDED IN LIST I 
       ARTICLE 7. Plants That Are Prohibited  
       It shall be prohibited to grow opium and corn poppies, cannabis and coca trees in Republic of Lithuania territory. 
       ARTICLE 8. The Lawful 
Circulation of the Substances Included in the    List 
       1. It shall be prohibited to 
use for health care purposes, the substances included in the list.
       2. It shall be prohibited to 
acquire, keep, transport within state territory, manufacture, process, import, 
export, use for scientific experimentation, the substances included in List I, 
without a license (permit) issued in accordance with the procedure established 
by the Republic of Lithuania Government.
       3. The Ministry of Health 
shall issue licenses according to Government established procedure, to acquire, 
keep, transport within State territory, manufacture, process, import, export and 
use for scientific experiments or law protection institutions, the required 
minimal amounts of the substances included in List I.
       4. The Ministry of Health 
shall establish the procedure of the lawful use for scientific purposes, of the 
substances included in List I. 
                   CHAPTER III 
THE REQUIREMENTS OF ACTIVITY INVOLVING THE SUBSTANCES INCLUDED IN LISTS II AND III 
       ARTICLE 9. General 
Requirements of the Lawful Use of Substances     Included in 
Lists II and III 
             
The activities involving the substances included in Lists II and III shall be 
applied the circulation requirements of other substances and preparations 
employed for health care and veterinary purposes, provided this Law shall not 
establish otherwise. 
             
ARTICLE 10. The licensing of Activities Involving the Substances 
    Included in Lists II or III 
       1. The substances included 
in Lists II and III may only be manufactured, imported into the Republic of 
Lithuania, exported from the Republic of Lithuania, engaged in wholesale or 
retail trade thereof in the Republic of Lithuania, by legal persons prepared for 
that activity, individual enterprises, having a licence for that activity, and 
only within the buildings and premises for the use of which a special license 
has been issued. 
       2. Issuance of licenses for 
the production, import into the Republic of Lithuania and export from the 
Republic of Lithuania of the substances included in Lists II and III and 
engaging in wholesale and retail trade thereof, interruption of the validity of 
these licenses, cancellation of interruption, procedure and conditions of 
re-registration and procedure of issuing licenses for the use of buildings or 
premises shall be established by the licensing regulations. The Government of 
the Republic of Lithuania shall confirm the regulations and establish the 
conditions of licensed activity. 
       3. Legal persons and 
individual enterprises may acquire and keep the narcotic and psychotropic 
substances included in Lists II and III, if they possess a licence to engage in 
pharmaceutical activity and a license for this activity, issued in accordance 
with the procedure established by the Government of the Republic of 
Lithuania.
       4. The Ministry of Health or 
an institution authorised by it, shall issue the licenses to manufacture, import 
into the Republic of Lithuania and export from the Republic of Lithuania the 
substances included in Lists II and III and engage in wholesale and retail trade 
thereof, interrupt the validity of these licenses, annul the validity and 
control licensed activity.
       5. A legal person or an 
individual enterprise may appeal to the Ministry of Health the decision 
regarding non issuance of license, interruption of its validity or annulment 
thereof, within a period of 30 calendar days. The Ministry shall examine the 
appeal within 30 days. A legal person or individual enterprise, if they are 
dissatisfied with the decision of the Ministry of Health, or if the Ministry of 
Health has failed to examine the appeal within the stipulated term, shall have 
the right to appeal to court.
       6. Having annulled the 
validity of a license, the remnants of the substances included on Lists II and 
III, held by a legal person or individual enterprise, shall be transferred to 
persons, holding a license to engage in activity with narcotic and psychotropic 
substances. 
       ARTICLE 11. Production of the Substances Included in Lists II and III  
       Licenses for production of the substances included in Lists I and II shall be issued only upon presentation of all of the documents regarding production and technological extraction processes, the projected amounts of production of the intermediate substances and composition thereof. The manufacturer must ensure that the production amounts indicated in the licence will not be exceeded. 
 
 
 
             ARTICLE 12. Trade in Substances Included in Lists II and III 
       1. Trade in substances included in Lists II and III shall be possible if they are properly packaged and marked.
       2. The Ministry of Health 
shall determine the specific requirements of the packaging and marking of the 
substances included in Lists II and III. 
       3. It shall be prohibited to 
trade in substances included in Lists II and III, packed in packaging that does 
not have the written names of substances, or if the markings appearing on the 
packaging are inaccurate.
       4. The names of substances, 
their amount, manner of use and warning concerning the required safety measures, 
must be indicated on the label.
       5. It shall be prohibited to 
sell substances included in Lists II and III, if due to unsuitable marking or 
unsuitable label (illegible inscription, damaged label etc.), because there are 
no accompanying documents or these are incomplete, it is possible to 
misunderstand the danger posed to health or their prescribed use (manner of 
use). 
       6. Persons engaged in 
wholesale marketing of the substances included in Lists II and III must register 
all of the sales facts in a special journal of a Ministry of Health approved 
form.
       7. Persons engaged in the 
wholesale marketing of substances included in Lists II and III must register, in 
accordance with the procedure established by the Ministry of Health, those who 
shall acquire these substances (natural person’s surname, first name, legal 
person’s or individual enterprise’s name, code, address), while the persons 
acquiring these, must submit the stipulated documents of registration. 
       8. The persons engaged in 
the wholesale marketing of the substances included in Lists II and III, must 
keep the documents according to which they have sold these substances, according 
to the procedure and terms stipulated by the Ministry of Health.
       9. Persons engaged in the 
wholesale marketing of the substances included in Lists II and III must submit 
the data of sales fact registration to an institution authorised by the Ministry 
of Health. The Ministry of Health or an institution authorised by it and law 
protection institutions shall have the right at any time to request that persons 
engaged in wholesale marketing of the substances included on Lists II and III, 
submit data regarding the sale of these materials.
       10. It shall be prohibited 
to sell the substances included in Lists II and III to persons not having a 
license for activity linked with narcotic and psychotropic 
substances. 
       ARTICLE 13. The Register 
       1. An institution authorised by the Ministry of Health shall administer the register of licenses which have been issued for production, import into the Republic of Lithuania, export from the Republic of Lithuania, engage in wholesale and retail marketing of substances included in Lists II and III and record the data on interruption and annulment of the validity of licenses.
       2. An institution authorised 
by the Ministry of Health shall annually establish the Republic of Lithuania’s 
need of the substances included in Lists II and III, administer the records of 
the production, import, export, wholesale and retail marketing, submit according 
to the established procedure, the requirement and lawful use of narcotic and 
psychotropic substances namely, accounting to the United Nations International 
Committee on Control of Narcotics. 
       ARTICLE 14. Conditions of 
Import, Export, and Transit of the     Substances Included 
in Lists II and III  
       1. The Government of the 
Republic of Lithuania guided by the international agreements of the Republic of 
Lithuania shall establish the conditions and implementation of import into the 
Republic of Lithuania, export from the Republic of Lithuania and transit across 
the territory of Lithuania of the substances included in Lists II and III.
       2. It shall be prohibited to 
store the substances included in Lists II and III in customs warehouses as well 
as temporarily keep them in import or export terminals. The customs procedures 
applied to temporary import, temporary import for processing, and processing 
under customs supervision may not be applied to these substances.
       3. Special permission of the 
Ministry of Health or its authorised institution shall be required in every 
individual instance of import or export of the substances included in Lists II 
and III. 
       4. Should the requirements 
of this Law or other legal acts, be violated in the course of importing, 
exporting or while in transit, the substances included in Lists II and III, the 
customs service shall apply all of the measures stipulated by laws, including 
interception and confiscation of these substances.  
       ARTICLE 15. Transportation 
Within the Territory of the Republic of     Lithuania of 
Substances Included in Lists II and III 
Persons, transporting the substances included in Lists II and 
III, within the territory of the Republic of Lithuania, must have accompanying 
freight documents and ensure the safety of said substances. Should a suspicion 
arise regarding possible unlawful use of substances included in Lists II and 
III, the person transporting the freight must bring this to the immediate 
attention of law protection institutions. 
       ARTICLE 16. Sending of Substances Included in Lists II and III 
       It shall be prohibited to send through the post, substances included in Lists II and III.  
 
CHAPTER FOUR 
ACQUISITION AND KEEPING OF SUBSTANCES INCLUDED IN LISTS II AND III  
       ARTICLE 17. Procedure of Ordering, Acquisition and Distribution of    Substances Included in Lists II and III in Pharmacies and    Health Care Institutions 
       1. The substances included 
in Lists II and III may be ordered for health care and veterinary science 
purposes only. The Ministry of Health shall establish the procedure of ordering 
(prescribing) such medicines. 
       2. A person having submitted 
a valid prescription for health care or veterinary purposes shall have the right 
to acquire at pharmacies the prepared substances included in Lists II and 
III.
       3. The Ministry of Health 
together with the State Veterinary Service shall establish the procedure for 
acquisition and distribution at pharmacies, of substances included on Lists II 
and III, for health care or veterinary purposes.
       4. The Ministry of Health 
shall establish the procedure of acquisition, prescription, issuance and record 
keeping of the substances, at health care institutions, 
       5. The substances included 
in Lists II and III shall be distributed for medicinal and veterinary purposes 
by those having the right to this activity:
       1) pharmaceutical 
specialists in retail marketing enterprises (pharmacies);
       2) pharmaceutical 
specialists in wholesale marketing and manufacturing enterprises;
       3) specialists in health care institutions;
       4) Veterinary and pharmaceutical specialists in veterinary service institutions.
       6. The requirements of 
health care and veterinary specialists, having the right to acquire, distribute 
the substances included on Lists II and III to perform their professional duties 
shall be established by the Ministry of Health along with the State Veterinary 
Service. 
       ARTICLE 18. Prescriptions of Substances Included in Lists II and III 
       1. Materials included in List II shall be prescribed on special prescription blanks. The Ministry of Health shall establish the form of special prescription blanks, their completion, record keeping and storing procedure.
       2. Materials included in 
List III shall be prescribed in accordance with the procedure established by the 
Ministry of Health.
       3. The sale of substances 
included in Lists II and III, according to an inappropriately completed 
prescription shall be prohibited. 
       ARTICLE 19. Medical First 
Aid Kits on International Travel Transport    Means 
       The substances included in 
Lists II and III which are contained in medical kits on international transport 
means for rendering necessary medical assistance, shall be stored according to 
the procedure established by the Ministry of Health. 
       ARTICLE 20. Passenger Rights 
       Passengers travelling across the Lithuanian border, may carry with them for personal consumption in connection with health care, accompanied by copies of the medicines prescribed for them, a supply of the substances included on List II, to cover a course of treatment of 7 days or less and of substances included on List III, to cover a treatment course of 30 days or less.  
       ARTICLE 21. Keeping of Substances Included on Lists II and III 
       1. The Ministries of Internal Affairs and Health shall establish the requirements of the premises where substances included in Lists II and III, shall be manufactured and the wholesale and retail trade shall be engaged in.
       2. The Ministry of Health 
shall establish the reserve quantities of substances included in Lists II and 
III, the procedure for keeping them in enterprises (pharmacies) for retail trade 
of medicines, enterprises for the wholesale trade in medicines, enterprises of 
medicine production, institutions of health care and veterinary service, 
laboratories of medicine control and scientific institutions.
       3. A person who has been 
prescribed for the care of his health, some of the substances included in Lists 
II and III, may keep no greater amount of these materials, than it was possible 
to acquire at the pharmacy, according to the prescription. 
       4.Persons who are keeping 
some substances included on Lists II and III, must protect them from any 
influence, which may alter their characteristics. The safety of these materials 
must be ensured totally and their packaging may not be damaged. 
       CHAPTER FIVE 
RECORDS AND CONTROL OF NARCOTIC AND PSYCHOTROPIC SUBSTANCE CIRCULATION  
       ARTICLE 22. The Entities of Record Administration and Control      of Narcotic and Psychotropic Substances Implementation 
       An institution authorised by 
the Ministry of Health Protection and other institutions authorised by the 
Government shall administer the records and control of narcotic and psychotropic 
substance circulation. 
             
ARTICLE 23. The Record-Keeping of the Circulation of Narcotic and 
    Psychotropic Materials 
       1. Guided by international 
agreements of the Republic of Lithuania the Ministry of Health, shall establish 
the procedure of record-keeping of narcotic and psychotropic substance 
circulation.
       2. The procedure for 
maintaining the records of narcotic and psychotropic substance inventorying and 
accounting of material values and the procedure of creating the balance of 
retail and wholesale enterprises and production enterprises shall be established 
by the Ministry of Health, guided by the provisions of the Law on the Principles 
of Accounting.
       Article 24. Records of 
Narcotic and Psychotropic Substance Circulation  An institution authorised 
by the Ministry of Health shall administer the records of narcotic and 
psychotropic substance circulation in the Republic of Lithuania and submit the 
accounting to the International Committee on Control of Narcotics Circulation. 
 
 
CHAPTER SIX 
FINAL PROVISIONS 
       ARTICLE 25. Liability 
 The person who shall be in violation of the requirements of this Law shall be liable in accordance with the procedure established by Republic of Lithuania laws. 
       Article 26. Proposal to the Government 
       The Ministry of Health shall prepare legislation in connection with this Law within three months of the coming into force of the Law on the Control of Narcotic and Psychotropic Substances. 
 
I promulgate this Law passed by the Seimas of the Republic of Lithuania. 
PRESIDENT OF THE REPUBLIC ALGIRDAS BRAZAUSKAS

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