Regulation amending the Regulation on veterinary medical products. Country/Territory Türkiye Document type Regulation Date 2020 Source FAO, FAOLEX Original source Official Gazette No: 31086, 1st of April, 2020. Subject Livestock Keyword Animal health Business/industry/corporations Certification Drugs Inspection Institution Internal trade International trade Monitoring Traceability/product tracing Public health Geographical area Asia, Black Sea, Europe, Europe and Central Asia, Mediterranean, Middle East, Western Asia Entry into force notes Article 9 of this Regulation enters into force six months after it is published in the Official Gazette and other provisions enter into force on the day it is published in the Official Gazette. Abstract This Regulation makes amendments regarding the inspection of premises and equipment intended to be used for manufacturing operations and storage, the control of starting and finished products, and the registration of importer and exporter of veterinary medicinal products to the veterinary medicinal product tracking systems. This Regulation adds provisions and makes amendments about the GMP (Good Manufacturing Practices) for veterinary medicinal products regarding certification and inspection of national and foreign manufacturers. Moreover, production sites, analysis laboratories, packaging facilities and release sites that provide contractual services for veterinary medicinal products are also subject to GMP inspections by the Ministry. In case a serious situation occurs that would endanger human and animal health or violation of the provisions of this Regulation, the Ministry may cancel the permit for production sites, in whole or in part, for certain pharmaceutical forms, or cancel all of them until contradictions are resolved. Full text Turkish Website www.resmigazete.gov.tr References - Legislation Amends Regulation on veterinary medical products. Legislation | Türkiye | 2011 Keyword: Drugs, Fish disease, Animal health Source: FAO, FAOLEX