1. — Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community…

1.

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 supervisory authorities shall have responsibility for verifying on behalf of the Community that the person responsible for placing the medicinal product on the market or the manufacturer or importer from third countries satisfies the requirements laid down in Chapter IV of Directive 75/319/EEC and for exercising supervision over such persons in accordance with Chapter V of Directive 75/319/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.