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Rules For The Illicit Manufacture Of Narcotic Drugs And Psychotropic Substances And Precursors, As Well As Procedures For The Movement Of Medicinal Plants, Herbal Lieltirgotav And Pharmacies

Original Language Title: Noteikumi par narkotisko un psihotropo zāļu un vielu, kā arī prekursoru aprites kārtību zāļu ražošanas uzņēmumos, zāļu lieltirgotavās un aptiekās

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Cabinet of Ministers Regulations No. 181 in Riga, July 4, 1995 (No. 36, 5. §) rules for the illicit manufacture of narcotic drugs and psychotropic substances and precursors, as well as procedures for the movement of medicinal plants, herb and pharmacy lieltirgotav issued in accordance with the law "on 1 April 1925 the law" the cabinet installation "restore" article 14 (3) (I). General Questions About Drugs and 1. psychotropic substances and medicines considered those substances and medicinal products (hereafter referred to as "substances and medicine") included in the Welfare Ministry's drug control Committee (hereafter referred to as "drug control Committee") under the supervision of existing drugs, psychotropic substances and precursors lists (annex 1).
2. This provision lists referred to in paragraph 1 (hereinafter referred to as "the list") and the controlled substance medications fall into the following areas: 2.1. prohibited narcotic drugs and psychotropic substances included in list I of the UN Convention of 1961 on narcotic substances (IV) list the classification and the United Nations Convention of 1971 on psychotropic substances in list I for classification;
2.2. the narcotic drugs and psychotropic medicine recognized as included in list II of the UN Convention of 1961 on narcotic substances of list I of the classification and the United Nations Convention of 1971 on psychotropic substances in list II and III classification;
2.3. psychotropic medicines included in list III of the UN Convention of 1971 on psychotropic substances list classification IV;
2.4. the precursors included in list IV under the 1988 United Nations Convention against narcotic drugs and psychotropic substances in tables I and II of the turnover.
3. the lists shall be published once a year in the Official Gazette. In the meantime, the list can be changed with the drug control Committee. Lists of the substances and herbal explanation is synonymous with drug control Committee.
4. the Ministry of welfare with a special order certain control measures may not be applied for preparations, incorporating substances within list II or III in tiny quantities and which are made in a way that does not raise the possibility of abuse.
5. Lists of the substances and drug chain order and synonymous with explanation of the pharmaceutical company, lieltirgotav or the pharmacy of medicines (hereinafter: the "company") provides the company the responsible pharmacist (pharmacies).
6. the head of the company according to the company's business nature, the layout of the premises and staff tasks orders on these provisions within the company. A copy of the order must be submitted to the drug control Committee.
7. the head of the company is legally responsible for the lists of substances, and the proper storage of the medicinal product, inventory, and order of service within the company.
8. the head of the company provides drug control Committee, pharmacy inspectors, representatives of the Ministry of the Interior or the drugs Bureau (hereafter referred to as ' drugs Office) employee free access to controlled substances and drugs, as well as the relevant documentation.
9. Pharmaceutical activities to list I substances is prohibited.
10. The pharmaceutical activity with annexes II and III, and IV of the list list of table I substances and medicinal products is allowed only to those companies that have the appropriate licence.
11. These terms must be in a visible place in enterprises, as well as premises storing lists of substances and medicines.
 
II. The illicit manufacture of narcotic drugs and psychotropic substances and drug storage 12. Room which holds the list of II and III substances and medicinal products (hereafter referred to as "space"), must be protected against the entry of persons not belonging to it, and looting.
The room must be the capital of a brick or concrete walls.
The room must be equipped with an alarm or connected to centralized security network.
Window should be barred or iestiklot with bruņustikl.
Room door must be of metal or finished with Tin.
Room ventilation should be ensured. Working with powdery substances and medicinal products must be carried out in a fume cupboard.
The entrance to the room where the substances in list II and medicine allowed only people who work with them. Room getting into an arc of persons in control of a company responsible pharmacist.
Space key kept by the pharmacist in charge of the company.
After working the room, the door must be locked or sealed and sealed must be connected to the alarm. Room lock, sealing or sealing order and key storage locations in the company's ceo is determined by written order.
13. List II substances and medicinal products must be stored in a safety deposit box. Safety must be array or fastened to the wall or floor space and fitted with an alarm.
14. List II substances and drug company in the area of movement outside the substance and drug storage space allowed only package, which does not belong to persons denied access to substances and medicines.
15. (iii) the list of substances and medicinal products must be stored in a lockable rooms (or cupboards lockers) separately from other substances and drugs.
 
III. The illicit manufacture of narcotic drugs and psychotropic substances and drug dispensing and receiving 16. List II substances and medicines are allowed to buy only lieltirgotav and pharmacies that have the appropriate licence, as well as medical institutions, which have received the drug control Committee permission to list II substances and drug purchases.
17. for the list of II and III substances and drugs for scientific purposes requires permission of drug control Committee.
18. the pharmacies that do not manufacture medicines of ekstemporāl Department, allowed to issue or receive only the shape of the finished product.
19. List II substances and medications to get the companies entitled to the Manager of the person. The company issued by the supervisor in the token is valid for 30 days. In all the powers "of the substances in list II and names of medicines and the quantity of numbers and words.
20. List II substances and medicinal products shall be issued only in sealed or sealed package. On the packaging indicates that the substance or the medicine seller and buyer. And internal packaging labelling of the medicinal product with two red stripes. List of substances and medicines only in the relevant accompanying document.
21. list II and III substances and drug orders and invoices article separately from other orders and invoices showing the volume of numbers and words.
List II substances and drug orders and invoices must be retained for a period of five years.
(Iii) the list of substances and drug orders and invoices must be retained for one year.
 
IV. The illicit manufacture of narcotic drugs and psychotropic substances and drug records

22. Any type of list II substances and medicine movement (shopping, transfer, export or import) should be recorded in the accounting books, which are typographic printed by the drug control Committee and the Ministry of welfare Pharmacy Department approved sample (annex 2).
23. plant accounting books, signed and stamped by the company responsible pharmacist (pharmacies) and with its stamp of approval to drug control Committee.
24. the records shall be made in the accounting books, leaving free space without deleting and overwriting. Each entry in the accounting book numbered and signed by the Manager of the company approved a certain person.
25. also to be recorded in the accounting books on fire, looting or other accident incurred losses and shall cause the accident. Records indicate the exact inventory of existing substances and the quantity of the medicinal product.
For damages must immediately inform the drug control Committee and the Office for combating drugs.
26. reference book also recorded the following substances in list III and the movement of medicinal products: 26.1. ephedrine (pure form or mixed with substances indiferent);
26.2. pseudo (pure form or mixed with substances indiferent);
26.3. the St.Johns;
26.4. ciklodol.
27. the drug control Committee order of individual substances and medicines containing one of these rules 26. substances listed in paragraph 1, may provide for other movements.
 
 
The notes.
1. reference book also other substances can be registered and the movement of medicinal products in accordance with Ministry of welfare Pharmacy Department's instructions.
2. Corrections to records with the words "Edit believe.", the signature of the person responsible and the seal of the company.
28. list II and III substances and drug residue, once a month, the Manager of the Phys. Invt ordered by the Commission. If the medicine shortage or surplus, as well as irregularities in the accounting records, the rooms must be sealed immediately by telephone and reported drug control Committee and the Office for combating drugs.
29. by paragraph 28 of these rules establish the facts referred to in the Enterprise Manager should immediately establish a Commission, which should include the following: 29.1. Drug Control Committee Member;
29.2. Drugs Office representative;
3. a representative of the pharmaceutical inspection;
29.4. the company's management representative;
29.5. the company responsible pharmacist.
30. This provision is referred to in paragraph 29, the Commission shall draw up a report and send it to the drug control Committee and the Office for combating drugs.
31. If the substances and herbal found looting or theft, immediately by telephone to report to the Office for combating drugs.
32. substances and medications that have expired or that otherwise does not comply with the regulatory and technical documentation requirements, stored in sealed separately from other substances and drugs and destroyed in the presence of the Commission, which is made up of included: 32.1. Drug Control Committee Member;
32. a representative of the pharmaceutical inspection;
32.3. the company's management representative;
32.4. the company responsible pharmacist.
33. The provision in paragraph 32, the Commission shall draw up, within three days to submit to the drug control Committee.
34. The companies for each of the substances in list II and III and the movement of medicinal products within the drug control Committee must submit the following reports: 34.1. the quarterly report (to be submitted within 15 days after the end of each quarter);
21.3. the report for the previous calendar year (must be submitted before 15 February).
 
 
Note the. The contents of the report depending on the nature of the business of the Ministry of welfare is determined.
 
35. During the year, the drug control Committee is entitled to request interim summaries.
 
 
V. rules for pharmaceutical companies and drug lieltirgotav-36. substances in list II and III and retail of medicinal products is prohibited.
37. Lists substances and medicines may be exported and imported, if you have received the drug control Committee.
38. Annexes II, III and IV of the list of substances and medicine imports, exports and transit operations each time you need the drug control Committee.
39. together with the substances in list II and medicine application for export permit drug control Committee must submit to the competent authorities of the importing State, the import authorization issued.
Together with the list of substances and III drug export permit application must be submitted to the competent authorities of the importing State, the import authorization issued, if this is provided for in national legislation or drug control Committee.
 
 
Vi. Rules of type and General Hospital (closed) pharmacies 40. License for opening and operation of pharmacies give rights to distribute all list III and IV medications. Pharmacy affiliates providing list III of substance and drug storage, and records in accordance with these provisions, have the right to distribute the medicines list III.
41. in order to carry out the activities under the pharmaceutical list II substances and medicines, the pharmacy must obtain a license. Pharmacy branches spread list II drugs are not allowed.
42. List II substances and medications stored in a safety deposit box not more than a month of consumption. Assistant room store substances and medicine not more than five days of consumption.
The General type of list II substances in pharmacies and medicines kept in safes in the rooms. Dežūraptiek the night safe storage of substances and quantities of medicinal products required for first aid. Banned list II substances and drug store sales.
43. List II substances and medicines to the room shall be a pharmacy assistant leader, or to the order of the head of the pharmacy appointed pharmacist who is responsible for the substances in list II and the movement of medicinal products.
44. List II drugs the patient is issued only against prescription, drawn on a special form, the model of which is determined by the Cabinet of Ministers, respectively. Prescribed therapeutic units ready-made medicines and doses of substances in list II drugs in pharmacies gatavotaj must specify the word.
45. the receipt of a valid prescription for medicinal products in seven days (if not Health Minister a special order for exceptions).
46. List II drugs a patient can get a pharmacy located in the hospital's operating region, which issued the prescription.
Medications that contain codeine, etilmorfīn and may be issued in any city or district concerned pharmacy.
47. The recipe specified in list II substances, necessary for the manufacture of medicinal products, separate issue is prohibited.
48. If a recipe drawn incorrectly, medicine issue is prohibited. Mistakenly discharged recipes recorded in special journals and destruction in every quarter.

49. list II drugs of the hospital's departments shall be issued against the request signed by the relevant head of Department and senior nurse. Prescribed therapeutic units ready-made medicines and doses of substances in list II drugs in pharmacies gatavotaj must specify the word.
50. the requests for medicinal products in list II are valid for seven days.
51. (II) the list of medicinal products recipes (requests) lists prescription (request) the registration book, which recorded and stamped the drug control Committee.
Prescription (request) the book of registration of these regulations shall also be recorded in paragraph 26 (iii) of the list of prescription medicines.
52. (II) the list of medicinal products recipes (requests) should be borne by the issuing of medicinal products in pharmacies and in five years should be maintained separate from your other recipes.
53. the accounting books and prescription (demand) registration book be maintained for ten years after the last entry to the competent authority without delay can be produced.
54. at the request of the patient, the pharmacist may be issued (II) and (iii) the list of medicinal products recipes that strike through Xerox with two diagonal stripes and bearing the notation "copy". It is given to patients who leave the country, or in other drug control Committee order in certain specific cases.
55. (iii) the list of substances and products are stored in closed form, separately from other substances and drugs.
The trading room to store substances and medicine not more than five days of consumption.
56. (iii) the list of medicinal products shall be issued against the request, or the recipe, drawn on a form, a model of which is determined by the Cabinet of Ministers, respectively.
57. The recipe (request) (iii) the list of medicinal products with a valid receipt within 30 days.
58. If the rules referred to in paragraph 26 (iii) of the list of medicinal products issued or made, it repeatedly noted in the registration book of recipes.
59. following the issuance of the prescription medicines (request) to keep the Pharmacy and store one year separately from other recipes.
Prime Minister m. cock Interior Minister j. Ādamson of annex 1 of the Republic of Latvia Ministry of welfare drug control Committee under the supervision of existing drugs, psychotropic substances and precursors lists these lists include 1 the narcotic drugs, psychotropic substances and precursors to the international non-proprietary name or with the applicable international conventions, as well as names mentioned: 1. specified substances lists the possible isomers, unless there are special exceptions;
1.2. specified substances lists possible esters and ethers, unless there are special exceptions;
1.3. specified substances in the lists of possible salt, including isomers, esters and ethers salt;
1.4. the medicinal products containing substances included on the list, unless these drugs are not included in the exceptions.
2. the lists under the 1961, 1971 and 1988 Conventions contained in the classification of a substance is broken down into four lists, with reference to the relevant Convention.
3. Substances listed in addition to the UN conventions mentioned or whose control provisions in the Republic of Latvia are more stringent than those laid down in the UN Convention, marked with an asterisk (*).
4. the official explanation and the list the name of the synonym is the transcript of the drug control Committee. List of replication allowed only kserokopēšan or photocopying.
 
(I) the list of particularly dangerous narcotic drugs and psychotropic substances, which prohibits the use of medical purposes 1961 Convention on narcotic substances list of Acetorfīn IV heroin — Alpha-methylfentanyl is Acetyl Ketobemidon Alpha-methylfentanyl 3-methylfentanyl is Alfacetilmetadol 3-metiltiofentanil beta-hidroksifentanil M P P P beta-hydroxy-3-methylfentanyl on the P Desomorfīn fluorfentanil-E A P a Tiofentanil Etorfīn in the 1971 Convention on psychotropic substances of list I Brolamfetamīn N-Ethyl-M-D A D E N T M A D D-hydroxy M A Paraheksil D M H P P M M A D T O D E T Psilocybin psilocin in the Etilciklidīn of the Roliciklidīn of cathinone S T P (D O M) (+)-Tenamfetamīn M D M lysergide (A) Tenociklidīn of mescaline ' nederwiet ' 4-Metilaminoreks T M A M M A D * Efedr * Efedron plant (metkatinon, metilkatinon) cannabis (hashish, anaš) of Cannabis resin in the poppy straw in poppy straw extract (concentrated) Tree Bush page * Jēlopij ' to list II dangerous narcotic drugs and psychotropic substances used for medical and scientific purposes the 1961 Convention on narcotic substances in the Etilmorfīn for Acetildihidrokodeīn I list of Etokseridīn of Acetilmetadol of Etonitazēn of Allilprodīn of Fenadokson Alfentanil in a Fenampromīd of Alfametadol Fenazocīn Alfameprodīn of metiltiofentanil of Fenomorfān of Alpha-Alfaprodīn in the Anileridīn Fenoperidīn of the Benzetidīn of Folkodīn of Benzilmorfīn of Fentanyl is a Betacetilmetadol Hidrokodon of Betameprodīn of Furetidīn of Hidromorfinol of Betametadol of Betaprodīn of Hidroksipetidīn of hydromorphone in the Dekstromoramīd of Klonitazēn Izometadon Benzitramīd of Dekstropropoksifēn of Diampromīd of Kodoksīm of codeine Dietiltiambutēn Difenoksīn Levofenacilmorfān cocaine is a Levometorfān of Dihidromorfīn Levomoramīd of dihydrocodeine in the Dimenoksadol of Levorfanol of Dimetiltiambutēn of Dimefeptanol of methadone methadone intermediate Dioksafetilbutirāt Metazocīn of the diphenoxylate Metildezorfīn is a Metildihidromorfīn in the Dipipanon of the Ekgonīn and Metopon Drotebanol derivatives of Etilmetiltiambutēn of Morferidīn Moramīd intermediate in the metobromīd of the Petidīn of morphine Morphine is morphine A intermediate N-oxide Petidīn Mirofīn of the Petidīn of the intermediate (B) intermediate in the Pimonidīn of the Nikodikodīn Nikokodīn C Piritramīd a Nikomorfīn Proheptazīn for a Noracimetadol for a Properidīn for a Norkodeīn for a Norlevorfanol Racemetorfān of Normetadon of Propirām of Racemoramīd of Normorfīn of Racemorfān of Norpipanon of Tebakon of oxycodone will Sufentanil metabolite of Tebaīn Tilidīn Petidīn of Trimeperidīn of opium in the 1971 Convention on psychotropic substances in list II Meklokvalon Deksamfetamīn amphetamine methamphetamine racemate of phencyclidine methamphetamine in Metakvalon Fenetilīn of Levamfetamīn of Sekobarbitāl methylphenidate Phenmetrazine in 1971 for the Convention on psychotropic Substances List III * * Amobarbitāl * * Katīn glutethimide buprenorphine * Butalbitāl * Pentazocīn * Ciklobarbitāl * Pentobarbitāl III list of dangerous psychotropic substances that can be used for malicious purposes, the 1971 Convention on psychotropic substances of Klonazepām Allobarbitāl list of IV Alprazolam Klorazepāt Amfepramon of Klotiazepām of Lefetamīn of Benzfetamīn of Loprazolām of a Barbitol in the Lorazepām of Butobarbitāl of Bromazepām of Delorazepām of Lormetazepām of Medazepām of Mazindol diazepam is a Mefenoreks Ethlorvinol of Meprobamāt Estazolam in the

Etinamāt is a Etilloflazepāt Metilfenobarbitāl of Etilamfetamīn of Midazolām of Fenkamfamīn methyprylon is a Fendimetrazīn of Nitrazepām of Nimetazepām of Nordazepām of Fenproporeks of Oksazepām St.johns is a Oksazolām of Fludiazepām Fenteramīn of Flunitrazepām of Pinazepām of Flurazepām pemoline is a Halazepām of Prazepām of Haloksazolam Pipradol is a Hlordiazepoksīd of Sekbutbarbitāl of Pirovaleron of Hlorazepāt of Kamazepām of Tetrazepām of Temazepām of Triazolām of Klobazām of Vinilbitāl Ketazolam * Cefedrīn * oksibutirāt * lithium * Mebikar * Ciklodol * sodium oksibutirāt Ephedrine * Fenazepām * * Fenatīn * Pseudo Sidnokarb * Grandaksīn * Sombrevīn IV list of precursors (substances frequently used in the illicit manufacture of narcotic drugs or psychotropic substances) the 1988 Convention against trafficking in drugs and psychotropic substances in table I of the turnover of the Claim of Lizergīnskāb 3,4 Ergometrine — metilēndioksifenil — 2-propanone, 1-phenyl-2-propanone N-acetylanthranilic acid is a Izosafrol Piperonāl Heksahidrodezoksiefedrīn a Safrole N-fenetil-4-anilinopiridīnij 4-anilīnopiridīn salt of N-fenetil-4-anilīnopiperidīn in the 1988 Convention against trafficking in drugs and psychotropic substances in table II turnover acetic anhydride, acetone methyl ethyl ketone piperidine ** anthranilic acid hydrochloric acid ** ether sulphuric acid ** Feniletiķskāb * * toluene potassium permanganate ** except this acid salt.
Interior Minister j. Ādamson annex 2 Interior Minister j. Ādamson in annex 3 Interior Minister j. Ādamson in