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Regulation on the procedure for expertise, testing and registration of veterinary drugs.

Country/Territory
Tajikistan
Document type
Regulation
Date
2012
Source
FAO, FAOLEX
Subject
Livestock
Keyword
Animal health Drugs Certification Registration Standards Internal trade Contract/agreement
Geographical area
Asia, Central Asia, CIS (Commonwealth of Independent States), Europe and Central Asia, Landlocked Developing Nations, North Asia
Abstract

This Regulation establishes the procedure for expertise, testing and registration of veterinary drugs. Veterinary drugs and other means for animal husbandry and veterinary science can be traded only by legal (physical) persons who have a license to sell veterinary drugs, obtained in accordance with the established procedure. Only veterinary drugs registered by the State Veterinary Supervision Service of the Ministry of Agriculture of the Republic of Tajikistan (SVMC) and certified, having a registration certificate and a certificate of compliance with the established standard shall be authorized for trade and application. Organization - developer or manufacture of veterinary drugs applies for registration (renewal of registration) to the competent authority. The application form must contain documentation listed in the Annexes 1, 2, 3. The applicant must conclude service contract with the competent authority and pay fees thereto. To conduct registration tests, the applicant must provide the necessary quantity of the drug and analytical standards. The registration certificate specifying the product name shall be issued for each medicinal product form. The registration certificate is valid for 5 years.

Full text
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