Community Code for Veterinary Medicinal Products Directive
Proposal for a EUROPEAN PARLIAMENT AND COUNCIL DIRECTIVE on the Community code relating to medicinal products for animal (codified version)
- Stage
- No longer in force
- Procedure
- Directive · Ordinary legislative procedure
- Last activity
- 18 Dec 2001
Documents
Newest first. Each opens at its source.
- Text adopted · OJ L 367 22.12.2006, p. 0033-0045Commission · 22 Dec 2006
- Text adopted · OJ L 349 12.12.2006, p. 0003-0014Commission · 12 Dec 2006
- Text adopted · OJ L 311 28.11.2001, p. 0001Commission · 28 Nov 2001
- Text adopted · Directive 2001/0082Commission · 6 Nov 2001
- OJ C 075 15.03.2000, p. 0011Commission · 15 Mar 2000
- Text adopted · 32006L0130Commission
- Text adopted · 32006R1950Commission
- Text adopted · T5-0365/2001Parliament
Summary
GeneratedDirective 2001/82/EC codifies EU rules on veterinary medicinal products, consolidating four earlier directives into a single text. It sets marketing authorization, manufacturing, wholesale distribution, prescription and pharmacovigilance obligations, including 15-day reporting of serious adverse reactions. It applies to manufacturers, authorization holders, wholesalers and veterinarians.
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Sources: EP Legislative Observatory · EU Law Tracker · EUR-Lex. Record as of 6 Oct 2026. Something wrong on this page? Report an error.
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