This content is exclusively provided by FAO / FAOLEX

Regulation (EC) No. 726/2004 of the European Parliament and of the Council laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency.

Country
Type of law
Legislation
Source

Abstract
The present Regulation establishes the procedures applicable to the authorization, supervision and pharmacovigilance of medicinal products for human and veterinary use. Title III is entirely devoted to the authorization and supervision of veterinary medicinal products. Article 30 provides for the setting up of the Committee for Medicinal Products for Veterinary Use, which shall be part of the European Medicines Agency established in accordance with Title IV hereto.
Date of text
Entry into force notes
The Regulation shall enter into force on 20 May 2004.
Repealed
No
Serial Imprint
Official Journal L 136, 30 April 2004, pp. 1-33.
Source language

English

Legislation Amendment
No