Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Regulation of veterinary medicines

Regulation of Veterinary Medicinal Products and Environmental Safety... [Pg.383]

Council Regulation (EC) No. 1308/1999 of 15 June 1999 amending Regulation (EC) No. 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin... [Pg.12]

R. Ancuceanu, Maximum residue limits of veterinary medicinal products and their regulation in European Community Law, Ear. Law J., 2003, 9, 215-240. [Pg.263]

Center for Veterinary Medicine (CVM). This center is responsible for the regulation and approval of animal food and dmg products. The center... [Pg.83]

A distinct concern arises in the area of veterinary dmgs because of the possibiUty that dmg residues may be conveyed to humans by the food-producing animals. Therefore, dmg residues and their safety in human food remain a central issue for the Center for Veterinary Medicine (CVM). Animal dmgs also include those products which promotional Hterature claims to improve feed efficiency and increase milk production. An animal food product is regulated under the 1968 Animal Dmg Amendments if it contains a dmg used in feed or premixes (25). [Pg.86]

Commission Regulation (EC) No. 1084/2003 of 3 June 2003 concerning the examination of variations to the terms of a marketing authorisation for medicinal products for human use and veterinary medicinal products granted by a competent authority of a Member State... [Pg.12]

Biologies (CVB), which is located within APHIS, is responsible for the review and licensing of such products. As outlined above, the CVM of the FDA regulates chemical-based veterinary medicines. [Pg.36]

The US regulates animal trials mainly through the requirement to inform the authorities before non-approved veterinary pharmaceuticals are shipped to trial sites. Depending on whether it is classified as a drug or a biologic, information must be submitted to either the FDA Center for Veterinary Medicines (CVM) or the United States Department of Agriculture (USDA) Center for Veterinary Biologies (CVB). [Pg.135]

APPLICATION FOR THE ESTABLISHMENT OF MRL(s) FOR AN ACTIVE SUBSTANCE TO BE USED IN VETERINARY MEDICINAL PRODUCTS IN ACCORDANCE WITH COUNCIL REGULATION (EEC)... [Pg.139]

See other pages where Regulation of veterinary medicines is mentioned: [Pg.28]    [Pg.39]    [Pg.117]    [Pg.182]    [Pg.78]    [Pg.346]    [Pg.469]    [Pg.115]    [Pg.153]    [Pg.333]    [Pg.1043]    [Pg.17]    [Pg.44]    [Pg.66]    [Pg.264]    [Pg.383]    [Pg.407]    [Pg.429]    [Pg.414]    [Pg.378]    [Pg.402]    [Pg.322]    [Pg.459]    [Pg.8]    [Pg.143]   


SEARCH



© 2024 chempedia.info