VETERINARY PHARMACOVIGILANCE IN THE UK
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Authors
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Giles Davis
Head of Pharmacovigilance Unit, Veterinary Medicines Directorate, Woodham Lane, New Haw, Addlestone Surrey, KT15 3LS, United Kingdom
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Nil
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K. N. Woodward BA, BSc (Jt Hons), MSc (Exp Pathol/Toxicol), MSc (Pharmacovigilance), PhD, CBiol, FIBiol, EurProBiol, CChem, FRSC, DipRCPath (Tox), MTOPRA, FBTS, Veterinary Pharmacovigilance – the UK Experience Veterinary Pharmacovigilance: Adverse Reactions to Veterinary Medicinal Products Published Online: 14 DEC 2009.
Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency. Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products. Volume 9B of The Rules Governing Medicinal Products in the European Union: Guidelines on Pharmacovigilance for Medicinal Products for Veterinary Use.
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All the copy right belongs to the sponsoring Organization, Tamil Nadu Veterinary and Animal Sciences University, Chennai - 51.
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