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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 structure and the amount of the fees referred to in Article 57 (1) shall be established by the Council acting under the conditions provided for by the Treaty on a proposal from the Commission, following consultation of organizations representing the interests of the pharmaceutical industry at Community level. CHAPTER 3 General provisions governing the Agency

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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.