Regulation (EC) No 726/2004 of the European Parliament and of the Councilof 31 March 2004laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency(Text with EEA relevance) (revoked)
TITLE IIAUTHORISATION AND SUPERVISION OF MEDICINAL PRODUCTS FOR HUMAN USE
TITLE IIIAUTHORISATION AND SUPERVISION OF VETERINARY MEDICINAL PRODUCTS
TITLE IVTHE EUROPEAN MEDICINES AGENCY — RESPONSIBILITIES AND ADMINISTRATIVE STRUCTURE

Regulation (EC) No 726/2004 of the European Parliament and of the Council

of 31 March 2004

laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency

(Text with EEA relevance) (revoked)

F1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .