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Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products · European Union

The granting of authorization shall not diminish the general civil and criminal liability in the Member States of the manufacturer or, where applicable, of the person responsible for placing the veterinary medicinal product on the market. CHAPTER 2 Supervision and sanctions

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Source: EUR-Lex (Cellar) · retrieved 2026-11-06 · Text as adopted (Official Journal); later amendments are not incorporated in this text.