preamble_19

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

Whereas, therefore, the exclusive responsibility for preparing the opinions of the Agency on all matters relating to medicinal products for human use should be entrusted to the Committee for Proprietary Medicinal Products created by the Second Council Directive 75/319/CEE; whereas in respect of veterinary medicinal products this responsibility should be entrusted to the Committee for Veterinary Medicinal Products created by Directive 81/851/EEC;

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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.