Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004
Laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency
(Text with EEA relevance)European Medicines Agency – EMA
- Recitals
TITLE I — DEFINITIONS AND SCOPE
TITLE II — AUTHORISATION AND SUPERVISION OF MEDICINAL PRODUCTS FOR HUMAN USE
TITLE III — AUTHORISATION AND SUPERVISION OF VETERINARY MEDICINAL PRODUCTS
TITLE IV — THE EUROPEAN MEDICINES AGENCY — RESPONSIBILITIES AND ADMINISTRATIVE STRUCTURE
TITLE V — GENERAL AND FINAL PROVISIONS
ANNEX