1990/0309(SYN)

Medicinal Products Authorization Regulation and European Medicines Agency

PROPOSAL FOR A COUNCIL REGULATION (EEC) 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

Stage: No longer in force
Procedure: Regulation · Cooperation procedure
Last activity: 30 Nov 1993

Summary

Generated

Regulation (EEC) No 2309/93 created the centralized Community procedure for authorizing medicinal products for human and veterinary use and established the European Agency for the Evaluation of Medicinal Products. Titles I, II, III and V entered into force on 1 January 1995, when the Agency took up its responsibilities.

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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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