Law-ref.org Convention on Psychotropic Substances
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manufacture [Global Index]


ARTICLE-1: USE OF TERMS     [go to this ARTICLE]
... (i) "Manufacture" means all processes by which psychotropic substances may be obtained, and includes refining as well as the transformation of psychotropic substances into other psychotropic substances. The term also includes the making of preparations other than those made on prescription in pharmacies. ...
... (j) "Illicit traffic" means manufacture of or trafficking in psychotropic substances contrary to the provisions of this Convention. ...


ARTICLE-2: SCOPE OF CONTROL OF SUBSTANCES     [go to this ARTICLE]
... (i) Require licences for manufacture, trade and distribution as provided in article 8 for substances in Schedule II; ...
... (i) Require licences for manufacture, trade and distribution in accordance with article 8; ...
... (i) Require licences for manufacture, trade and distribution in accordance with article 8; ...
... (i) Require licences for manufacture, trade and distribution in accordance with article 8; ...
... 9. The Parties shall use their best endeavours to apply to substances which do not fall under this Convention, but which may be used in the illicit manufacture of psychotropic substances, such measures of supervision as may be practicable. ...


ARTICLE-3: SPECIAL PROVISIONS REGARDING THE CONTROL OF PREPARATIONS     [go to this ARTICLE]
... (a) article 8 (licences), as it applies to manufacture; ...
... (d) article 15 (inspection), as it applies to manufacture; ...


ARTICLE-4: OTHER SPECIAL PROVISIONS REGARDING THE SCOPE OF CONTROL     [go to this ARTICLE]
... (b) The use of such substances in industry for the manufacture of non-psychotropic substances or products, subject to the application of the measures of control required by this Convention until the psychotropic substances come to be in such a condition that they will not in practice be abused or recovered; ...


ARTICLE-5: LIMITATION OF USE TO MEDICAL AND SCIENTIFIC PURPOSES     [go to this ARTICLE]
... 2. Each Party shall, except as provided in article 4, limit by such measures as it considers appropriate the manufacture, export, import, distribution and stocks of, trade in, and use and possession of, substances in Schedules II, III and IV to medical and scientific purposes. ...


ARTICLE-7: SPECIAL PROVISIONS REGARDING SUBSTANCES IN SCHEDULE 1     [go to this ARTICLE]
... (b) Require that manufacture, trade, distribution and possession be under a special licence or prior authorization; ...


ARTICLE-8: LICENCES     [go to this ARTICLE]
... 1. The Parties shall require that the manufacture of, trade (including export and import trade) in, and distribution of substances listed in Schedules II, Ill and IV be under licence or other similar control measure. ...
... (a) Control all duly authorized persons and enterprises carrying on or engaged in the manufacture of, trade (including export and import trade) in, or distribution of substances referred to in paragraph 1; ...
... (b) Control under licence or other similar control measure the establishments and premises in which such manufacture, trade or distribution may take place; and ...


ARTICLE-11: RECORDS     [go to this ARTICLE]
... 1. The Parties shall require that, in respect of substances in Schedule 1, manufactures and all other persons authorized under article 7 to trade in and distribute those substances keep records, as may be determined by each Party, showing details of the quantities manufactured, the quantities held in stock, and, for each acquisition and disposal, details of the quantity, date, supplier and recipient. ...
... 1. The Parties shall require that, in respect of substances in Schedule 1, manufactures and all other persons authorized under article 7 to trade in and distribute those substances keep records, as may be determined by each Party, showing details of the quantities manufactured, the quantities held in stock, and, for each acquisition and disposal, details of the quantity, date, supplier and recipient. ...
... 2. The Parties shall require that, in respect of substances in Schedules II and III, manufacturers, wholesale distributors, exporters and importers keep records, as may be determined by each Party, showing details of the quantities manufactured and, for each acquisition and disposal, details of the quantity, date, supplier and recipient. ...
... 2. The Parties shall require that, in respect of substances in Schedules II and III, manufacturers, wholesale distributors, exporters and importers keep records, as may be determined by each Party, showing details of the quantities manufactured and, for each acquisition and disposal, details of the quantity, date, supplier and recipient. ...
... 5. The Parties shall require that, in respect of substances in Schedule IV, manufacturers, exporters and importers keep records, as may be determined by each Party, showing the quantities manufactured, exported and imported. ...
... 5. The Parties shall require that, in respect of substances in Schedule IV, manufacturers, exporters and importers keep records, as may be determined by each Party, showing the quantities manufactured, exported and imported. ...
... 6. The Parties shall require manufacturers of preparations exempted under paragraph 3 of article 3 to keep records as to the quantity of each psychotropic substance used in the manufacture of an exempt preparation, and as to the nature, total quantity and initial disposal of the exempt preparation manufactured therefrom. ...
... 6. The Parties shall require manufacturers of preparations exempted under paragraph 3 of article 3 to keep records as to the quantity of each psychotropic substance used in the manufacture of an exempt preparation, and as to the nature, total quantity and initial disposal of the exempt preparation manufactured therefrom. ...
... 6. The Parties shall require manufacturers of preparations exempted under paragraph 3 of article 3 to keep records as to the quantity of each psychotropic substance used in the manufacture of an exempt preparation, and as to the nature, total quantity and initial disposal of the exempt preparation manufactured therefrom. ...


ARTICLE-15: INSPECTION     [go to this ARTICLE]
... The Parties shall maintain a system of inspection of manufacturers, exporters, importers, and wholesale and retail distributors of psychotropic substances and of medical and scientific institutions which use such substances. They shall provide for inspections, which shall be made as frequently as they consider necessary, of the premises and of stocks and records. ...


ARTICLE-16: REPORTS TO BE FURNISHED BY THE PARTIES     [go to this ARTICLE]
... (a) In regard to each substance in Schedules I and II, on quantities manufactured, exported to and imported from each country or region as well as on stocks held by manufacturers; ...
... (a) In regard to each substance in Schedules I and II, on quantities manufactured, exported to and imported from each country or region as well as on stocks held by manufacturers; ...
... (b) In regard to each substance in Schedules III and IV, on quantities manufactured, as well as on total quantities exported and imported; ...
... (c) In regard to each substance in Schedules 11 and III, on quantities used in the manufacture of exempt preparations; and ...
... (d) In regard to each substance other than a substance in Schedule I, on quantities used for industrial purposes in accordance with sub-paragraph (b) of article 4.The quantities manufactured which are referred to in sub-paragraphs (a) and (b) of this paragraph do not include the quantities of preparations manufactured. ...
... (d) In regard to each substance other than a substance in Schedule I, on quantities used for industrial purposes in accordance with sub-paragraph (b) of article 4.The quantities manufactured which are referred to in sub-paragraphs (a) and (b) of this paragraph do not include the quantities of preparations manufactured. ...