Name of law a law amending the law on the control of narcotic substances and precursors of the Name Bill a bill amending and supplementing the law on control of narcotic substances and precursors of acceptance Date 05/03/2010 number/year Official Gazette 22/2010 Decree No 53
On the grounds of art. 98, paragraph 4 of the Constitution of the Republic of Bulgaria
I DECLARE:
To be published in the Official Gazette the law amending the law on the control of narcotic substances and precursors, adopted by the National Assembly of the HLI, 5 March 2010.
Issued in Sofia on 12 March 2010.
The President of the Republic: Georgi Parvanov
Stamped with the State seal.
Minister of Justice:
Margarita Popova
LAW
amending the law on the control of narcotic substances and precursors (promulgated, SG. 30 of 1999; amend. and Suppl., no. 63 of 2000, issue 74, 75 and 120 of 2002, no. 56 of 2003, issue 76, 79 and 103 by 2005, issue 30, 75 and 82 of 2006, no. 31 and 55 of 2007. , PC. 36, 43 and 69 by 2008 and PC. 41, 74, 82 and 93 from 2009.)
§ 1. In art. 5 is hereby amended as follows:
1. In the text before paragraph 1 the word "Preparations" shall be replaced by "medicinal products".
2. In paragraph 1 the word "preparation" is replaced by "medicinal product".
§ 2. In art. 9, para. 3, after the words "Minister of health" a comma and add "Minister of agriculture and food".
§ 3. In art. 9 a, paragraph 1, after the word "licences" insert "and" permissions.
§ 4. In chapter one creates art. 9:
"Art. 9. Minister of agriculture and food is the admin of: 1. revenues from the fees for the issue of permits and licences for activities under art. 29 and article. 35, para. 1;
2. revenue from fines and financial penalties imposed under this Act by the supervisory authorities to the Minister of agriculture and food. "
§ 5. In art. 10 is hereby amended as follows:
1. In paragraph 8. 3 the word "two" shall be replaced by "three".
2. in the Al. 4, the words "of the drug agency" shall be deleted.
3. in the Al. 5, the words "can participate and representatives of non-governmental" are replaced by "cast and representatives of non-profit organizations, medical institutions, registered under the medial institutions act".
§ 6. In art. 11 is hereby amended as follows:
1. point 1 shall be amended as follows:
1. defining and coordinating national policy in the field of narcotic substances and precursors, shall draw up and propose to the Council of Ministers to adopt a national strategy to combat substance abuse and against illicit traffic in narcotic drugs and precursors for a period of 5 years; ".
2. In paragraph 2 the word "accept" is replaced by "offers of the Council of Ministers to adopt".
3. Point 7 is replaced by the following:
7. determine and approve the national drug coordinators and the national coordinator of international programs and projects in the field of drugs; ".
§ 7. In art. 13, para. 1, paragraph 3, the word "led" is replaced by "coordinate".
§ 8. Article 15 shall be amended as follows:
"Art. 15. (1) the municipal councils are created by drugs and preventive information centers to them in the municipalities, which are administrative centers of areas. The Organization and activities of the councils and centers are determined by the regulation for the Organization and activities of the National Council on narcotic substances.
(2) Advice on narcotic drugs under para. 1 develop, provide and coordinate the implementation of municipal programmes to combat substance abuse.
(3) Preventive information centers under para. 1 carry out preventive activities and programs, harvested, stored and analysed the information necessary for the implementation, coordination and preparation of programmes under para. 2.
(4) Advice on narcotic substances under para. 1 informacioni and preventive centres are financed with funds from the State budget through the municipal budgets as delegated by the State activities.
(5) the municipal councils of municipalities which are not administrative centers of areas, may create committees on narcotic drugs, which are financed with private funds from municipal budgets.
(6) the municipal councils under para. 1 can perform methodological activity for the development of the prevention of the use of narcotic drugs in the municipalities of Pará. 5, in which there is no established committees on drugs. "
§ 9. In art. 15A, para. 1 the words "coordinate and" are deleted.
§ 10. In art. 16, al. 1 Finally after the figure "3" a comma and add "as well as on the treatment of persons dependent on narcotic substances".
§ 11. Art is created. 16A:
"Art. 16. (1) the Minister of education, youth and science and the Minister of health carry out controls on prevention of the use of narcotic substances.
(2) the Minister of health and Minister of labour and social policy carried out a control on the psychosocial rehabilitation of persons addicted to drugs.
(3) in carrying out the checks at al. 1 and 2, the Minister of health is assisted by officials from the National Center for addictions to the Ministry of health. "
§ 12. In art. 17 paragraph. 3:
"(3) the control of the country's territory on the treatment of persons dependent on narcotic drugs, shall be carried out by employees of the regional health centers with higher medical education."
§ 13. In art. 18, al. 2 the words "Ministry of finance" shall be replaced by "Customs Agency to the Minister of finance" and the words "Ministry of Justice and the State Agency for national security" shall be replaced by the words "and the Department of Justice."
§ 14. In art. 21, after the word "transit" is added "from and to third countries."
§ 15. In art. 22 the word "32A" is replaced by "35".
§ 16. Article 23 is hereby repealed.
§ 17. In art. 27 the following modifications are made:
1. Paragraph 1 shall be amended as follows:
"(1) it is prohibited to the sowing and cultivation on the territory of the Republic of Bulgaria of opium plants, the coca bush and the plants of the hemp (cannabis), except in the cases of art. 29, para. 1. "
2. in the Al. 3 the words "tetrahydrocannabinol content above 0.2%, determined in foliage, flower and fruit tips" are deleted.
§ 18. Article 29 shall be amended as follows:
"Art. 29. (1) the keeping, semeproizvodstvoto, import and export of plants and seeds from the hemp (cannabis) in the content of 0.2% tetrahydrocannabinol, definitely in the foliage, flower and fruit kernels, as well as imports and exports of opium shall be carried out only after authorisation issued under conditions and by an order determined by an Ordinance of the Minister of agriculture and food.
(2) approval of importers of hemp and hemp seed other than for sowing, and the issue of a licence for the importation of hemp and hemp seed other than for sowing under art. 5, paragraph 2, third indent, of Regulation (EC) no 1673/2000 of 27 July 2000 on the common organisation of the markets in flax and hemp grown for fibre shall be subject to the conditions and in the order specified by an Ordinance of the Minister of agriculture and food. "
§ 19. The title of chapter v shall be replaced by the following: "control of narcotic substances and medicinal products containing narcotic substances in annexes 2 and 3 and of precursors of narcotic drugs".
§ 20. In art. 32, para. 1 the word "made" is replaced by "perform", and the words ' the Council ' shall be replaced by "Minister of health".
§ 21. Article 32a shall be replaced by the following:
"Art. 32a. (1) persons applying for a licence under art. 32, para. 1, submitted to the Ministry of health sample application that apply: 1. a copy of the authorisation for production or marketing authorisation for wholesale of medicinal products issued pursuant to the law on medicinal products for human use;
2. the certificate of criminal record of the applicant – sole proprietor or to the Manager/Executive Director of the legal person and the applicant – pharmacists under art. 34;
3. a document issued by the respective district operations, stating that the applicant against – sole proprietor, Manager or Executive Director of the legal person who is the applicant, and against the master-pharmacist under art. 34 there is no charge for an indictable offence;
4. a copy of the judgment for registration and certificate of good standing, tax registration, and registration at BULSTAT, for persons registered or re-registered under the law on the commercial register, indicating the unified identification code;
5. a document issued by the registry agency or from the Court Registry of the applicant – a trader that he is declared bankrupt or is not in bankruptcy proceedings;
6. a document issued by the registry agency or from the Court Registry of the applicant – legal person, that he is not in liquidation;
7. certificate issued by the tax office, on the presence or absence of public debts to the State;
8. a copy of the document to the right of ownership or the right to use the site, in which the activities will be carried out with drugs and medicinal products containing narcotic substances;
9. approved by the Chief Architect of the municipality of architectural design of the buildings and spaces in which activities will be carried out with narcotic drugs;
10. a copy of the guard with the Ministry of the Interior or the natural or legal person holding an authorisation to carry out the private security activity, and a copy of this permit;
11. list of narcotic substances, which will carry out the activities referred to in the application;
12. instruction for activities with drugs and medicinal products containing narcotic substances, approved by the persons referred to in item 2;
13. order of sole trader or managing the company to determine the persons responsible for the execution of activities directly with narcotic drugs;
14. diploma of higher education in the specialty "Pharmacy" of pharmacists under art. 34;
15. a document certifying that the master-responsible pharmacist under art. 34 functions have been assigned to implement the obligations set out in the licence;
16. document for paid fee in the amount set out in the tariff referred to in art. 9, para. 3.
(2) manufacturers of medicinal products containing narcotic substances, shall apply in addition to the documents referred to in para. 1 and:
1. a copy of the permission for use of medicinal products containing narcotic substances which produce the producer concerned;
2. Description of the technological process (technological scheme for production of drugs) and a brief description of the machines and equipment that will be used in the production and processing of narcotic drugs and medicinal products containing narcotic substances;
3. a copy of the material-the norms of technological regulation for the production of each medicinal product containing narcotic substances.
(3) wholesalers submit copies of all documents and the Inspector on narcotic substances in the regional center of health in the field of activity concerned.
(4) the narcotic drugs inspectors to the appropriate regional health center in the area, within the territory of which the buildings and premises where the activities will be carried out in wholesale trade, carry out on-the-spot check to establish conformity of actual conditions with the requirements of the law and the Ordinance under art. 32, para. 1 and shall draw up a report in two copies.
(5) the Protocol of verification under paragraph 1. 4 is officially forwarded to the Ministry of health shall, within 5 days from the date of completion of the inspection.
(6) in the investigation under paragraph 1. 4 can participate and experts from the Directorate for Narcotic Substances "of the Ministry of health.
(7) the experts of the Directorate of al. 6 carry out on-the-spot inspection of the buildings and spaces in which activities will be carried out in production and storage of narcotic substances and medicinal products containing narcotic substances, establishing the conformity of the actual conditions with the requirements of the law and the Ordinance under art. 32, para. 1 and shall draw up a report in two copies.
(8) when establishing the deficiencies in the documents presented or discrepancy between the status of buildings and premises, and the requirements laid down in the Ordinance under art. 32, para. 1 for carrying out the checks referred to in paragraph 1. 4 and 7, the Director of the Directorate "narcotic drugs" shall notify the applicant and give instructions for their removal.
(9) in the cases referred to in para. 8 deadline for issue of the licence shall be suspended until the removal of deficiencies and/or discrepancies.
(10) the Minister of health on the basis of a proposal from the Directorate for narcotic drugs "shall issue a licence for the production, processing, storage, wholesale trade in the country of import, export and transit, transfer and transport of narcotic drugs and/or medicinal products containing narcotic substances or makes reasoned refusal to issue within two months from the filing date of the application."
§ 22. Art is created. 32 (b):
"Art. 32B. (1) the licence referred to in art. 32, para. 1 shall be entered:
1. the purpose and date of issue/renewal;
2. name, registered office and Head Office of the person receiving the licence;
3. the type of activities and the term of the licence;
4. the address of the premises and the type of premises which are produced, processed, stored or marketed wholesale drugs and medicinal products containing narcotic substances, as well as requirements for their safety;
5. the list of narcotic substances, carrying out the activities;
6. the type of accountability;
7. full names of pharmacists – head of the stock under art. 197, paragraph 2 of the law on medicinal products for human use;
8. full name and particulars of the identity document of the person responsible under art. 34.
(2) in the Ministry of health is leading a special register of licences issued under art. 32, para. 1.
(3) in the registry under para. 2 fit the data referred to in para. 1. "
§ 23. Article 33 shall be amended as follows:
"Art. 33. (1) the retail and storage of medicinal products containing narcotic substances in annexes 2 and 3, shall be carried out with a licence issued by the Minister of health or from authorized by him Deputy Minister under conditions and by an order determined by the Ordinance under art. 32, para. 1.
(2) the licence referred to in paragraph 1. 1 is issued to a person who has obtained permission for opening a pharmacy pursuant to the law on medicinal products for human use. "
§ 24. Create art. 33 a-33 (d):
"Art. 33. (1) persons applying for a retail licence under art. 33, para. 1, submitted to the Ministry of health, sample application, to which apply:
1. the certificate of criminal record of the applicant – sole proprietor, Manager or Executive Director of the entity and of the master-pharmacist under art. 34;
2. a document issued by the respective district operations, stating that the applicant against – sole proprietor, Manager or Executive Director of the legal person who is the applicant, and against the master-pharmacist under art. 34 there is no charge for an indictable offence;
3. a copy of the judgment for registration, certificate of good standing, tax registration, and registration at BULSTAT, for persons registered or re-registered under the law on the commercial register, indicating the unified identification code;
4. a document issued by the registry agency or from the Court Registry of the applicant – a trader that he is declared bankrupt or is not in bankruptcy proceedings;
5. a document issued by the registry agency or from the Court Registry of the applicant – legal person, that he is not in liquidation;
6. a certificate issued by the tax office regarding the presence or absence of public debts to the State;
7. higher education diploma in the specialty "Pharmacy" of pharmacists under art. 34;
8. a copy of the guard with the Ministry of the Interior or the natural or legal person holding an authorisation to carry out the private security activity, and a copy of this permit;
9. instructions for carrying out activities with drugs, approved by the persons referred to in para. 1, item 1;
10. an order determining the person or persons responsible for the execution of activities directly with narcotic drugs;
11. a document certifying that the master-responsible pharmacist under art. 34 functions have been assigned to implement the obligations set out in the licence;
12. document for paid fee in the amount set out in the tariff referred to in art. 9, para. 3.
(2) copies of any documents shall be made available to the Inspector and the narcotic substances in the regional health center in the area, in whose territory is situated the pharmacy.
(3) After the submission of the documents for the issuance of a licence for retail and storage of medicinal products containing narcotic substances, narcotic drugs inspectors to the Regional Centre for health carried out an on-the-spot check to establish conformity of actual conditions with the requirements of the law and of the Ordinance under art. 32, para. 1 and shall draw up a report in two copies.
(4) the minutes of the examination under paragraph 1. 3 is sent officially to the Ministry of health shall, within 5 days from the date of completion of the inspection.
(5) upon establishment of the deficiencies in the documents presented or discrepancy between the status of buildings and premises, and the requirements laid down by the Ordinance under art. 32, para. 1 at the time of the examination under paragraph 1. 3, Directorate for narcotic drugs "shall notify the applicant and give instructions for their removal.
(6) in the cases referred to in para. 5 the term for the issue of a licence shall be suspended until the removal of deficiencies and/or discrepancies.
(7) the Supreme Council of pharmacy to the Minister of health will make a proposal for granting or refusing a licence in al. 1.
(8) the Minister of health in accordance with the proposal of the Supreme Council of pharmacy issued a licence for retail and storage of medicinal products containing narcotic substances, or reasoned refused issue within two months of receipt of the application.
Art. 33 (b) (1) the licence referred to in art. 33, para. 1 shall be entered:
1. the purpose and date of issue;
2. name, registered office and Head Office of the person receiving the licence;
3. the type of activities that will be carried out;
4. the location of the pharmacy in which retail and storage of medicinal products containing narcotic substances;
5. the type of accountability;
6. name of pharmacists – head of the Pharmacy;
7. the name and identity document of pharmacists under art. 34.
(2) in the Ministry of health is leading a special register of licences issued under art. 33, para. 1.
(3) in the registry under para. 2 fit the data referred to in para. 1.
Art. 33. (1) within 10 days of any change in the circumstances referred to in the licences referred to in art. 32, para. 1 and art. 33, para. 1, the licensee shall submit an application in accordance with art. 32 and, according to art. 33A, applying the change-related documents.
(2) the application and the documents attached to it in the Al. 1 is considered by the procedure of art. 32 and 33A.
(3) the Minister of Health issued a licence with reflected changing or reasoned refused issue within two months of receipt of the application referred to in paragraph 1. 1. (4) in the event of a change of pharmacists under art. 34, entered in the licence under art. 33, para. 1 the holder of the licence stops retail with medicinal products containing narcotic substances from the point of suspension of the fulfilment of the obligations under art. 34 from the established licence-master pharmacist.
Art. 33. (1) for the renewal of a licence referred to in art. 32, para. 1 persons shall submit an application to the Ministry of health within three months before the expiry of the period of validity to her, as the documents referred to in art. 32 a, para. 1.
(2) upon renewal of the licence, in the event that no changes have occurred, persons and submit Declaration in a form approved by the Minister of health, without submitting the documents referred to in art. 32 a, para. 1, item 8 and 9.
(3) the renewal of a licence shall be made within the time limits and in accordance with art. 32A. "
§ 25. Article 34 shall be amended as follows:
"Art. 34. licences under art. 32, para. 1 and art. 33, para. 1 shall be issued to a natural or legal person registered as a dealer under the Bulgarian legislation or the legislation of a Member State of the European Union, provided that the activities with narcotic substances in annexes 2 and 3, as well as with medicinal products containing narcotic drugs shall be carried out under the guidance of a master pharmacist who is responsible for the implementation of the measures provided for in the law and in the licence. "
§ 26. New art. 35: "art. 35. (1) the production, processing, storage, trade, imports and exports of narcotic drugs of no 2 and 3 applications for veterinary medicinal purposes shall be carried out after the issuance of a licence by the Minister of agriculture and food.
(2) the licences referred to in paragraph 1. 1 shall be issued to a natural or legal person registered as a dealer under the Bulgarian legislation or under the legislation of another Member State of the European Union, provided that the activities with narcotic substances in annexes 2 and 3, as well as with medicinal products containing narcotic drugs shall be carried out under the direction of the veterinarian responsible for the implementation of the measures provided for in the law and in the licence.
(3) the requirements and conditions for carrying out the activities referred to in para. 1 shall be determined by an Ordinance of the Minister of agriculture and food. "
§ 27. New art. 36:
"Art. 36. (1) persons applying for a licence under art. 35, para. 1, submit to the Director-General of the national veterinary service sample application, which contains:
1. the name and address or name, seat and address of management of the applicant;
2. the location of the buildings and the premises where the activities will be carried out with drugs and medicinal products containing narcotic substances;
3. the type of activities that will be carried out;
4. the name and particulars of the ID of the veterinarian under art. 35, para. (2);
5. unified identification code (UIC).
(2) an application under subsection. 1 shall apply:
1. a copy of the licence for the production or wholesale licence or retail with veterinary medicinal products issued pursuant to the law on animal health activities;
2. the certificate of criminal record of the applicant – sole proprietor or to the Manager or Executive Director of the legal person and the applicant – the veterinarian under art. 35, para. (2);
3. copy of diploma of the veterinarian under item 2;
4. a document issued by the respective district operations, stating that the applicant against – sole proprietor, Manager or Executive Director of the legal person, or against a veterinarian under art. 35, para. 2 there is no charge for an indictable offence;
5. a document issued by the registry agency or from the Court Registry of the applicant – a trader that he is declared bankrupt or is not in bankruptcy proceedings;
6. a document issued by the registry agency or from the Court Registry of the applicant – legal person, that he is not in liquidation;
7. certificate issued by the tax office, on the presence or absence of public debts to the State;
8. a copy of the judgment for registration and certificate of good standing, tax registration, and registration at BULSTAT, and persons registered or re-registered under the law on the commercial register, indicating the UIC;
9. a copy of the Act of putting into operation of the site in which the activities will be carried out with drugs and medicinal products containing narcotic substances, issued under the law on spatial planning;
10. copy of the document of title or right of use of the site, in which the activities will be carried out with drugs and medicinal products containing narcotic substances;
11. a copy of the guard with the Ministry of the Interior or the natural or legal person holding an authorisation to carry out the private security activity, and a copy of this permit;
12. list of narcotic substances and medicinal products containing narcotic substances, which will carry out the activities referred to in the application;
13. a copy of the instructions for carrying out activities with drugs and medicinal products containing narcotic substances, approved by the applicant under item 2;
14. a copy of the warrant of the sole trader or managing the company to determine the persons responsible for the execution of activities directly with drugs and medicinal products containing narcotic substances;
15. a document certifying that the responsible veterinarian are assigned functions in the implementation of the obligations set out in the licence;
16. document for paid fee in the amount set out in the tariff referred to in art. 9, para. 3. (3) persons who carry out production under art. 35, para. 1, apply to the documents referred to in para. 2 and:
1. Description of the technological process (technological scheme for production of narcotic substances and medicinal products containing narcotic drugs) and a brief description of the machines and equipment that will be used in the production and processing of narcotic drugs and medicinal products containing narcotic substances;
2. a copy of the material-the norms of technological regulation for the production of each medicinal product containing narcotic substances. "
§ 28. Create art. 36A-36 is:
"Art. 36. (1) the Director of the national veterinary service with a fixed Commission, which examines the documents referred to in art. 36, carry out on-the-spot check to establish conformity with the requirements of the law and the Ordinance under art. 35, para. 3 and be drawn up in duplicate.
(2) in establishing the deficiencies in the documents presented or discrepancy between the status of buildings and premises, and the requirements laid down by the Ordinance under art. 35, para. 3, the Commission shall inform in writing the applicant and give instructions for their removal.
(3) in the cases referred to in para. 2 the term for the issue of a licence shall be suspended until the removal of deficiencies and/or discrepancies.
(4) the Commission under para. 1 issue an opinion to the Director-General of the national veterinary service.
(5) the Director General of the National Veterinary Office on the basis of the opinion of the Commission shall submit to the Minister of agriculture and foodstuffs proposal for a licence or for a motivated refusal to issue.
(6) the Minister of agriculture and food on the basis of the proposal referred to in paragraph 1. 5 issued a licence for the production, processing, storage, wholesale or retail, import and/or export of narcotic drugs and medicinal products containing narcotic substances, or reasoned refuses issue within three months from the filing date of the application.
(7) the refusal under para. 6 may be appealed pursuant to the administrative code.
Art. 36 (b) (1) the licence referred to in art. 35, para. 1 shall be entered:
1. the purpose and date of issue/renewal;
2. the name and address or name, seat and address of management of the person who has obtained the licence;
3. the type of activities that will be carried out, and the term of the licence;
4. the location of the buildings and premises in which are produced, processed, stored or marketed in wholesale or retail drugs and medicinal products containing narcotic substances;
5. the type of accountability;
6. the name of the veterinarian under art. 35, para. 2.
(2) The licence referred to in paragraph 1. 1 list of narcotic substances and medicines containing narcotic substances, which will carry out the activities referred to in the application.
Art. 36. the Licence shall be served personally on the applicant or his authorised representative with a notarized power of attorney a person.
Art. 36. (1) the holder of a licence for activities under art. 35, para. 1 or his authorised representative shall submit an application to the Director-General of the national Veterinary Office of any change of circumstances referred to in the licence, by the order of art. 36.
(2) the application shall be accompanied by the documents relating to the change.
(3) the Director General of the National veterinary service with a fixed Commission in the event of a change in circumstances:
1. under art. 36 (b), para. 1, 2, 5 and 6 shall check the documentation to the application by the procedure of art. 36 a, para. 1-4 without on-the-spot check;
2. under art. 36 (b), para. 1, item 3 and 4 and al. 2 check under art. 36, para. 1-4, including an on-the-spot check.
(4) the Director General of the National Veterinary Office on the basis of the opinion of the Commission shall submit to the Minister of agriculture and foodstuffs proposal for issue of licence for addition to or motivated refusal to issue.
(5) the Minister of agriculture and food on the basis of the proposal referred to in paragraph 1. 4 issue a supplement to the licence or makes reasoned refusal to issue within:
1. two months from the filing of the application for a change of circumstances-under par. 3, item 1;
2. three months from the filing of the application for a change of circumstances-under par. 3, item 2.
Art. 36 (1) for the renewal of a licence shall submit an application to the persons the Director-General of the national Veterinary Office within three months before the expiry of the period of validity of her applying the documents referred to in art. 36 a, para. 2, item 1 – 8, 11 and 16.
(2) the renewal of a licence shall be accompanied by the Minister of agriculture and food on the proposal of the Director-General of the national Veterinary Office after verification by the procedure of art. 36 a, para. 1-4.
Art. 36. (1) in the national veterinary service shall keep a register of licences issued for activities involving drugs for veterinary medicinal purposes of annexes 2 and 3.
(2) the register referred to in para. 1 fit the data under art. 36 (b) and (c) data relating to the change of circumstances in the original licence issued. "
§ 29. Article 37 shall be amended as follows:
"Art. 37. (1) the licences referred to in art. 32, para. 1 and art. 35, para. 1 shall be issued for a period of three years from the date of issue, the licence referred to in art. 33, para. 1 is indefinite.
(2) the licence and certificate of registration under art. 18 (a), para. 2 are personal and may not be transferred or ceded.
(3) the licences referred to in art. 32, para. 1 and art. 33, para. 1 shall be served personally on the applicant or the authorized person after submission of the notarized power of attorney. "
§ 30. Article 38 shall be amended as follows:
"Art. 38. (1) in the Ministry of economy, energy and tourism public records shall be kept for the licences and certificates of registration.
(2) the register of issued licences for activities involving precursors of the first category contains:
1. the name of the licensed company;
2. address;
3. the number of the licence;
4. the period of validity of the licence.
(3) the register of issued certificates of registration for activities involving precursors from the second and third category contains:
1. name of the registered company;
2. address;
3. the number of the registration;
4. date of issue of the certificate of registration. "
§ 31. Article 39 shall be replaced by the following: "art. 39. By 31 January each year, the holders of a licence for retail and storage of medicinal products containing narcotic substances, presented in the regional center of health declaration that there is no change in the circumstances under which the licence was issued, and that no circumstances have arisen under art. 41, para. 1. "
§ 32. Article 40 shall be replaced by the following:
"Art. 40. Natural and legal persons having obtained a licence under art. 32, para. 1, art. 33, para. 1 and art. 35, para. 1 may acquire, transfer or distribute narcotic substances in annexes 2 and 3 only to persons holding a licence under this Act. "
§ 33. Article 41 shall be amended as follows:
"Art. 41. (1) the Minister of health may issue an order for the revocation of the licence under art. 32, para. 1 and art. 33, para. 1 in the following cases:
1. If the requirements of the law;
2. failure to comply with the conditions set out in the licence;
3. After setting the misrepresentation referred to in issue;
4. after the issuance of an order under art. 99 for the prohibition of activities;
5. in charge of deliberately an indictable offence or a final judgment of a deliberate crime against the physical person – sole proprietorship, or against the responsible person for the performance of activities under art. 34;
6. at the request of another State in connection with a request for legal assistance in the investigation, prosecution or judicial proceedings against the person abroad.
(2) an order for forfeiture of the licence shall be issued regardless of the imposition of administrative penalties.
(3) on the expiry of one year from the withdrawal of the licence under paragraph 1. 1, item 1 – 4 the person may reapply for receipt of the licence by the procedure of art. 32 and 33A.
(4) where the persons referred to in para. 1, item 5 are rehabilitated, they may apply again to obtain a licence in accordance with art. 32 and 33A.
(5) after the termination of the criminal proceedings under para. 1, item 5, as well as in case of the grounds referred to in paragraph 1. 1, item 6 restores the Health Minister at the request of the licence under paragraph 1. 1.
(6) upon the revocation of the licence under paragraph 1. 1 or on expiry of the period of its action in respect of stocks shall apply the procedure under art. 45.
(7) not consuming a legal person issued under art. 32, para. 1 licence for the production and storage, where a ground under para. 1, item 5. In the case of a final judgment the management bodies of a legal person within 7 days of notification, take action to change a Manager/Executive Director and/or the responsible person for the performance of activities under art. 34.
(8) No licence shall be withdrawn under art. 33, para. 1 the medical establishment for hospital care in the event of grounds under para. 1, item 5. The head of the hospital in 7 days is taking action to change the head of pharmacy. "
§ 34. Article 42 shall be amended as follows:
"Art. 42. (1) where, on the basis of art. 41, para. 1, item 1 – 4 and 6, when the licence is issued by the Minister of agriculture and food, the supervisory authorities of the national Veterinary Office made a proposal to the Director-General of the national Veterinary Office for her withdrawal.
(2) in establishing the basis of Pará. 1 from another public body it shall immediately notify the Director-General of the national veterinary service.
(3) in the cases referred to in para. 2 the Director General of the National veterinary service with a fixed Commission, which carried out the verification of the circumstances referred to in the notification.
(4) the results of the examination under paragraph 1. 3 the Commission shall deliver an opinion to the Director General of the national veterinary service.
(5) on the basis of the data referred to in para. 1 or the opinion of the Commission, thus confirming the existence of the grounds referred to in paragraph 1. 1, the Director of the national veterinary service will make a proposal to the Minister of agriculture and food for the withdrawal of the licence.
(6) the Minister of agriculture and food on the basis of the proposal referred to in paragraph 1. 5 issue a reasoned order for the withdrawal of the licence.
(7) the order for withdrawal of the licence may be appealed pursuant to the administrative code.
§ 35. Article 43 shall be amended as follows:
"Art. 43. the surrender and withdrawal of a licence issued under art. 32, para. 1 and art. 33, para. 1 subject to appeal pursuant to the administrative code.
§ 36. Article 44 is amended as follows:
"Art. 44. licences under art. 32, para. 1, art. 33, para. 1 and art. 35, para. 1 shall terminate:
1. with the expiry of the period for which they are issued, and in the event that their holders apply for renewal;
2. at the request of their holders, submitted to the issuing authority;
3. upon the death of pharmacists, registered as a sole proprietor and licensed by the procedure of art. 33, para. 1;
4. upon termination of the licence for manufacture of medicinal products or the authorisation for wholesale trade of medicinal products or of the authorization for the opening of a pharmacy, issued in accordance with the law on medicinal products for human use;
5. upon termination of the sole trader or activity of the legal person and the cancellation of the registration. "
§ 37. Articles 44 and 45 (b) are repealed.
§ 38. Article 45 shall be replaced by the following:
"Art. 45. (1) within 14 days of the termination of the licence referred to in art. 44, and the revocation of the licence or the suspension of a licence or registration for activities involving precursors of first and second category at the request of the operator to the Interministerial Commission for the control of precursors or upon the death of the natural person – sole proprietorship, the supervisory authorities shall carry out an inspection of buildings and premises where activities were carried out with narcotic substances in annexes 2 and 3, and no precursor of first and second category as well as the documentation. Special registers are transmitted to keep the Government body which issued the licence.
(2) within three months of the completion of the inspection, the individuals or their descendants, as well as legal persons can provide your warehouse stocks of persons granted a licence under this Act, inform the Department of health respectively, the Ministry of agriculture and food or the Interministerial Commission for the control of precursors at the Minister of economy, energy and tourism.
(3) Holders of a licence for retail and storage of medicinal products containing narcotic substances, may grant pursuant to para. 2 stocks are stocks only to persons who have received a licence under this Act, not later than two months from the completion of the inspection.
(4) after the expiry of the period referred to in para. 2 stocks of narcotic substances in annexes 2 and 3 shall be destroyed by the order of art. 97, while stocks of precursors of the first and second category shall be destroyed under the control of the Interministerial Commission for the control of precursors at the Minister of economy, energy and tourism. The costs of destruction shall be borne by the persons referred to in para. 2. "
§ 39. Articles 45A to 45 c is repealed.
§ 40. In art. 46 the following modifications are made:
1. In paragraph 8. 1 the words "art. 32 "is replaced by" article. 32, para. 1 and art. 35, para. 1. "
2. in the Al. 3 the word "only" is deleted.
§ 41. In art. 47, para. 6, after the word "import" and "export is added.
§ 42. In art. 54, para. 2, after the word "licence" shall be added "and persons engaged in the import and export of narcotic drugs for the purpose of allowing for the use of the medicinal product or the clinical trial".
§ 43. In chapter v the name of section IV is amended as follows: "the Requirements in trade and storage of narcotic substances in annexes 2 and 3, prescription, dispensing and possession of drug products containing narcotic drugs".
§ 44. Article 55 shall be amended as follows:
"Art. 55. (1) the right to purchase and retain narcotic substances in annexes 2 and 3 and medicinal products containing narcotic substances have only persons approved under art. 32, para. 1, art. 33, para. 1 and art. 35, para. 1.
(2) the supply and storage of medicinal products containing narcotic substances in special warehouses of the State medical reserve and in wartime stocks of the Ministry of the Interior and the Ministry of defence shall be carried out after authorisation by an order determined by the Ordinance of the Council of Ministers. "
§ 45. In art. 56 after the word "grant" is added "medicinal products containing narcotic drugs".
§ 46. In art. 57 after the word "quantity" is added "medicinal products containing".
§ 47. In art. 58 following amendments and supplements shall be made:
1. In paragraph 8. 1, after the word "hold" is added "medicinal products containing".
2. in the Al. 2 the words "recipe or" shall be deleted.
§ 48. In art. 59 following amendments and supplements shall be made:
1. In paragraph 8. 1 the words "import and export" shall be replaced by "carry for personal use containing medicinal products".
2. in the Al. 2 the words "document" shall be replaced by "authorized", and the words "for import and export of narcotic drugs" shall be deleted.
3. in the Al. 3 the word "Document" is replaced by "Authorization".
4. a para. 4:
"(4) medicinal products containing narcotic drugs under para. 1, can be worn only by the persons to whom they are prescribed. "
§ 49. In art. 60 is made the following changes and additions:
1. Paragraph 1 shall be amended as follows:
' (1) medicinal products containing narcotic substances in annexes 2 and 3, are prescribed by an order determined by the Ordinance of the Minister of health. "
2. in the Al. 2 the words "narcotic drugs and psychotropic" are replaced by "medicinal products containing narcotic drugs".
3. in the Al. 3, after the words "reporting of" add "medicinal products containing" and the word "narcotic" is replaced by "narcotic drugs".
4. in the Al. 4 after the word "prescribe" insert "containing medicinal products".
§ 50. In art. 61, para. 1, after the word "substances" insert "and medicinal products containing narcotic drugs".
§ 51. In art. 63, para. 1 the words "and their preparations" shall be replaced by the words "medicinal products containing narcotic substances, as well as".
§ 52. In art. 65 words "15 days" shall be replaced by the words "10 days" and the words "their preparations" shall be replaced by the words "medicinal products containing narcotic drugs".
§ 53. In art. 65 and the words "15 days" shall be replaced by the words "10 days" and the words "their preparations" shall be replaced by the words "medicinal products containing narcotic drugs".
§ 54. In art. 65 (b) the following amendments and supplements shall be made:
1. In paragraph 8. 1, after the word "available" is added "medicinal products containing the" and the words "and their preparations" shall be deleted.
2. in the Al. 3 the words "drugs and their preparations" shall be replaced by the words "medicinal products containing narcotic drugs".
§ 55. Create art. 65 c and 65 d: "art. 65. Within 10 days after the end of each quarter, the persons engaged in the import and export of narcotic drugs under art. 46, para. 3 and 4, shall submit a report on the imported and exported drugs in the Directorate for Narcotic Substances "of the Ministry of health.
Art. 65. Within 30 days after the end of each calendar year, the Ministry of the Interior and the Ministry of defense shall submit a report in "Drugs Directorate of the Ministry of health for handling of medicinal products containing narcotic substances in special warehouses of the State medical reserve and wartime stocks."
§ 56. In art. 66 the words "their preparations" shall be replaced by the words "medicinal products containing narcotic drugs".
§ 57. In art. 68 following amendments and supplements shall be made:
1. In paragraph 8. 1, after the words "packages of" insert "containing medicinal products" and the word "narcotic" is replaced by "narcotic drugs".
2. in the Al. 2 the first sentence shall be replaced by the following: "For medicinal products containing narcotic substances, the packaging must be marked with two diagonal red bands, for medicinal products containing psychotropic substances – with two blue strips."
3. Paragraphs 4 and 5 are repealed.
§ 58. In art. 69, after the words "transfer of" insert "medicinal products containing the" and the words "and their preparations" shall be deleted.
§ 59. Article 70 is amended as follows:
"Art. 70. it is prohibited to direct and indirect public advertising of narcotic substances and plants of applications Nos 1, 2 and 3 and medicinal products containing narcotic substances. "
§ 60. In art. Al 73. 1 shall be amended as follows:
"(1) for medical and educational purposes, scientific and laboratory tests, as well as for the maintenance of the working condition of service dogs, revealing drugs, permission is granted to natural and legal persons to produce, acquire, import, export, store, use, and apply limited amounts of plants and substances referred to in annexes n ° 1, 2 and 3 and their preparations and precursors."
§ 61. In art. 74 the word "authorization" is replaced by "authorization".
§ 62. In art. 80 is made the following changes and additions:
1. The current text becomes paragraph 1.
2. Al are created. 2-4:
"(2) at the National Center for addictions national focal point is created as part of the European information network on drugs and drug addiction, supporting the European Monitoring Centre for drugs and drug addiction.
(3) the national focal point in al. 2 builds and maintains a public information system on drugs and drug addiction, as well as early-warning information system for new drugs as part of the European early warning system.
(4) the functions and tasks of the national focal point shall be determined by the regulation for the National Center on addiction. "
§ 63. The title of Chapter 7 shall be replaced by the following: "prevention, treatment and psychosocial rehabilitation of persons dependent or abusing drugs.
§ 64. In art. 84 following amendments and supplements shall be made:
1. Paragraphs 1 and 2 shall be read with the following adaptations:
(1) the Ministry of health, Ministry of education, youth and science, the Ministry of labour and social policy, Ministry of defence, the Ministry of physical education and sport and the State Agency for child protection in accordance with their competence, provide, develop and implement programmes to reduce the demand for drugs, which include: prevention of the use of narcotic drugs, treatment and psychosocial rehabilitation of persons abusers or dependent on drugs and harm reduction from the use of narcotic substances.
(2) The persons who are dependent or abusing drugs, providing access to treatment programs, psychosocial rehabilitation and harm reduction from the use of narcotic drugs. "
2. in the Al. 3 Add "and hospitals registered under the medial institutions act".
§ 65. Create art. 84A and 84 (b):
"Art. 84. The conditions and procedures for the implementation of programmes for the prevention of narcotic drugs shall be determined by an Ordinance of the Minister of health and Minister of education, youth and science.
Art. 84 b. rules for the implementation of programmes to reduce the harm from the use of narcotic drugs shall be determined by an Ordinance of the Minister of health. "
§ 66. Article 85 shall be replaced by the following:
"Art. 85. (1) every Bulgarian citizen is entitled to treatment and psychosocial rehabilitation for addiction or abuse of narcotic drugs.
(2) the Department of health establishes a system for the collection, processing, analysis and dissemination of information about treatment programs and psychosocial rehabilitation.
§ 67. Art is created. 85A:
"Art. 85. (1) to the Minister of health created the expert advice on treating addictions, which discusses and gives opinions on:
1. the main directions and priorities in the field of treatment of addictions;
2. draft standards for good practice in the treatment of addictions and the proposals for changes in the current standards for good practice in the treatment of addictions;
3. the draft regulations in the field of the treatment of addictions;
4. new methods and treatment programs;
5. proposals for inclusion of new medicinal products containing narcotic substances (agonists and opievi agonist-antagonists) in the list used for the treatment of addictions programs for treatment with agonists and antagonists-agonist;
6. inclusion in treatment programs for persons who do not meet the criteria set out in the standards of good practice in the treatment of addictions;
7. clinical, professional, ethical issues and issues related to the application of standards of good practice and the work of healing programs.
(2) the Expert Council on addictions treatment consists of 11 members and includes: Deputy Minister of health, who is Chairman of the Board, two representatives of the Ministry of health, the Director of the National Center on addiction, at least one habilitirano person working in the field of addictions treatment, at least four doctors working in the field of the treatment of addictions and other specialists.
(3) the Minister of health shall determine by order of the Council composition under subsection. 2.
(4) the functions and organization of the activities of the Expert Council under para. 1 shall be determined by regulations issued by the Minister of health. "
§ 68. In art. 86 following amendments and supplements shall be made:
1. Paragraph 1 shall be amended as follows:
(1) coordination and methodological guidance on activities related to the prevention of the use of narcotic drugs, treatment and psychosocial rehabilitation of persons or dependent abusers of narcotic substances, and reduce damage from the use of narcotic drugs shall be carried out by the National Center on addiction to the Ministry of health. "
2. a new paragraph. 2:
"(2) the specialized control of the healing activity is carried out by the National Center on addiction, as the territory of the country is assisted by regional health centers of the Ministry of health."
3. The current paragraph. 2 it al. 3.
§ 69. Article 87 shall be amended as follows:
"Art. 87. (1) agonist treatment programs and agonist-antagonists of persons dependent on opioids, to be carried out with the authorisation issued by the Minister of health or from authorized by him Deputy Minister, under conditions and by an order determined by an Ordinance of the Minister of health.
(2) the Minister of health may refuse the authorisation subject to the conditions and procedures laid down in the Ordinance referred to in para. 1.
(3) the refusal of the Minister of health to issue a permit subject to appeal pursuant to the administrative code.
§ 70. Create art. 87 a-87 in:
"Art. 87. Authorization under art. 87, para. 1 shall cease:
1. with the expiry of the period for which it is issued, if the holder has not made an application for its renewal;
2. at the request of the holder, submitted to the Minister of health.
Art. 87B. Health Minister or authorized by him Deputy Minister, issued the authorization under art. 87, para. 1 may withdraw it, in the following cases:
1. in any systematic violations of the terms and conditions for the implementation of programs for the treatment with agonists and antagonists-agonist, determined by the Ordinance under art. 87, para. 1;
2. where systematic violations of standards of good practice for the treatment of the syndrome of dependence to opioids with agonists and antagonists-agonist;
3. failure to comply with the conditions laid down in the authorisation;
4. in establishing the misrepresentation referred to in issue.
Art. 87. (1) at the National Center on addiction creates and maintains the official database of the persons included in the programs for the treatment with agonists and antagonists-agonist.
(2) the database under para. 1 contains:
1. unique identification code of the person;
2. medicinal product used in the treatment of the person;
3. date of entry and the name of the hospital, performing treatment program with agonists and antagonists-agonist;
4. date of discharge from the treatment program with agonists and antagonists-agonist.
(3) the conditions and procedures for creating and using professional database under para. 1 shall be determined by the Ordinance under art. 87, para. 1. "
§ 71. In art. 88 following amendments and supplements shall be made:
1. Paragraph 1 shall be amended as follows:
(1) the participation of persons or dependent abusers of drugs in treatment programmes for psychosocial rehabilitation and harm reduction is based on the principles of voluntary participation and privacy as information is provided to persons and services only in the cases provided for in law. "
2. in the Al. 4, the words "Individual or collective" shall be deleted and the word "cure" is replaced by "Treatment".
3. a para. 5:
"(5) the treatment of minors, dependent or abusing drugs, carried out with their informed consent, and with the consent of a parent or guardian."
§ 72. Article 89 shall be amended as follows.
"Art. 89. (1) the programmes for the psychosocial rehabilitation of persons who were dependent on or abuse of narcotic substances, shall be carried out:
1. the institutions and persons referred to in art. 18 of the Act on social assistance;
2. from the clinic for specialized medical care – an individual practice for specialized medical and psychiatric help for medical group practice specialized psychiatric help, medical centre and diagnostic-consultative Center when held in a home environment;
3. in hospitals for inpatient psychiatric help and the dispensaries for psychiatric diseases, when held in the izv″ndomašna environment.
(2) the conditions and procedures for the implementation of programmes for the psychosocial rehabilitation shall be determined by an Ordinance of the Minister of health and Minister of labour and social policy. "
§ 73. In art. 91 following amendments and supplements shall be made:
1. In paragraph 8. 1 the words "Ministry of finance" shall be replaced by "to the Minister of finance by order, specified by an Ordinance of the Council of Ministers, and".
2. in the Al. 2, the words "to store" shall be deleted, and after the words "customs" shall be added by the order of the Ordinance under para. 1. "
§ 74. In art. 92 is hereby amended as follows:
1. The first subparagraph of paragraph 1 shall be repealed.
2. in the Al. 2 the words "the entry into force of conviction or until the expiry of the time limits for the discharge of the prosecution" shall be replaced by the words "termination of the criminal proceedings as appropriate.
§ 75. In art. 93 is hereby amended as follows:
1. In paragraph 8. 1 the words "tetrahydrocannabinol content above 0.2%" shall be deleted.
2. paragraph 2 is replaced by the following:
"(2) the plants shall be destroyed on the spot by the order of the Ordinance under art. 91, para. 1. "
§ 76. In art. 95 following amendments and supplements shall be made:
1. In paragraph 8. 1 the words "Council of Ministers" shall be replaced by "by the Ordinance under art. 91, para. 1. "
2. paragraph 2 is repealed.
3. Paragraph 3 is replaced by the following:
"(3) the destruction under para. 1, except in the cases under art. 93, is done by a Committee, composed of representatives of the national investigation service, the Customs Agency, the Directorate for narcotic substances "of the Ministry of health and General Directorate for fighting organised crime."
4. a para. 4:
(4) all documents related to the destruction of the plants, narcotic substances, their preparations and representative samples shall be kept for 4 years from the date of the destruction. "
§ 77. In art. 96 is hereby amended as follows:
1. In paragraph 8. 1 the word ' Surveillance ' is replaced by ' for the purpose of destroying the observers ".
2. in the Al. 2 the word "Court" is replaced by "for the purposes of destroying Court".
§ 78. In art. 97 the words "their preparations" shall be replaced by the words "medicinal products containing narcotic drugs".
§ 79. Article 101 is replaced by the following:
"Art. 101. Who does not comply with the requirements of art. 29, is punishable by a fine of 5000 to 50 000 LV. "
§ 80. Article 102 shall be replaced by the following:
"Art. 102. That does not comply with the rules for prescribing and dispensing of medicinal products containing narcotic substances in annexes 2 and 3 determined by the Ordinance under art. 60, para. 1, is punishable by a fine of 500 to 1000 BGN, and for repeated infringement – with fine 5000 BGN, if not subject to more severe punishment. "
§ 81. In art. 103 the number "1000" shall be replaced by "5000".
§ 82. Article 104 shall be amended as follows:
"Art. 104. That does not comply with the requirements for the marking of narcotic substances and medicinal products containing narcotic substances is punishable by a fine of 10 000 to 30 000 BGN, and for repeated infringement – a fine of 30 000 to 50 000.
§ 83. In art. 105 the number "1000" shall be replaced by "5000".
§ 84. In art. 106 the number "1000" shall be replaced by "5000".
§ 85. In art. 107 and the number "1000" shall be replaced by "5000".
§ 86. (B) Article 107 shall be amended as follows:
"Art. 107 b. who carries out activities in violation of art. 89, para. 1 shall be punishable by a fine of 20 000 to 50 000.
§ 87. In art. 108 the number "1000" is replaced by "20 000".
§ 88. In art. 108 and the figure "500" is replaced by "2000".
§ 89. In art. 109 the number "10000" is replaced by "50000".
§ 90. In § 1 of the supplementary provision the following amendments and additions:
1. In paragraph 13, the word "means" is replaced by "products".
2. In paragraph 16, finally a comma and add "not including production.
3. point 20 shall be replaced by the following:
"20." program for treatment with agonists and antagonists-agonist ' shall mean prescribing (opievi agonists or antagonists-agonist) in combination with a wide range of medical and psychosocial services to relieve the adverse medical, psychological and physiological effects attributed to opioidnata dependency, under conditions and in accordance with procedures specified by the Minister of health. "
4. In paragraph 11 (a) the words "customs territory" shall be replaced by ' the '.
5. In paragraph 23 (b), the words "customs territory" shall be replaced by ' the '.
6. Create is that 29-32:
"29." direct advertising "means any form of commercial message, communication or recommendation, which aims the promotion of drugs and/or their use through the use of the substances themselves or actions associated with their use, production and/or distribution.
30. "Indirect advertising" means any form of commercial message, communication, recommendation or action that uses the name and/or an image representing or approximating drug advertising on goods and promotional products.
31. "systematic violations" are three or more violations of the terms and conditions for the implementation of programs for the treatment with agonists and antagonists-agonist, determined by the Ordinance under art. 87, para. 1, or standards of good practice for the treatment of the syndrome of dependence to opioids with agonists and antagonists-agonist.
32. the "special register" means a register of Dan s which are intended for official use only. "
§ 91. In annex 1 to the art. 3, al. 2, after the word "Acetorfin" is added "1-benzyl piperazine", after the "Beta-hidroksifentanil" add "4-Bromo-2.5 dimetoksifenilamin", after "DOET" is added "2.5-dimethoxy-4-jodofenetilamin (2C-I), 2.5-dimethoxy-4-etiltiofenetilamin (2C-T-2), 2.5-dimethoxy-4-(n)-propiltiofenetilamin (2C-T-7)" after "4-" metilaminoreks "is added to 4-metiltioamfetamin (4-MTA)" after the word "Opium" is added "para-metoksimetamfetamin (PMMA)", after "TMA" is added "2, 4, 5-trimetoksiamfetamin (TMA-2) and" after the word "Fenetilin" is added "Fenilpiperazin and its halogen derivatives".
§ 92. In annex 2 to the art. 3, al. 2, after the word "Codeine" insert "Codeine-N-oxide.
§ 93. In annex 3 to the art. 3, al. 2 after the word "insert" Butalbital 1.4-Butanediol, "after" Vinilbital "is added" gamma-butyrolactone, gamma-hydroxybutyrate "," added "gamma-hidroksibutirova acid", after "Ketazolam" is added after the ketamine and "Haloksazolam" is added "Chloral hydrate".
Transitional and final provisions
§ 94. Regional advice on narcotic substances in the municipalities, which are administrative centers of areas, continue to operate and are renamed in the municipal councils in narcotic substances.
§ 95. The Customs Agency drugs, plants and preparations at the established order that has not been drawn up gear-reception Protocol and criminal proceedings is complete as appropriate, shall be destroyed within 6 months from the entry into force of this law.
§ 96. Within one year of the entry into force of this Act, a Committee of representatives of the Ministry of health, through the Directorate for narcotic substances "of the Ministry of health, the Ministry of finance through the Customs Agency, Ministry of the Interior through the relevant structure, the Sofia city prosecutor and Metropolitan investigation service destroys data stored by the Department of health drugs.
§ 97. (1) within four months of the entry into force of this law, the competent authorities shall issue the normative acts for its implementation.
(2) pending the entry into force of the acts under paragraph 1. 1 normative acts issued for the implementation of the law shall apply, in so far as they do not contradict it.
The law was adopted by 41-Otto National Assembly on 5 March 2010 and is stamped with the official seal of the National Assembly.
President of the National Assembly Tsetska Tsacheva:
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