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
- Recitals
TITLE I — DEFINITIONS AND SCOPE
TITLE II — AUTHORIZATION AND SUPERVISION OF MEDICINAL PRODUCTS FOR HUMAN USE
TITLE III — AUTHORIZATION AND SUPERVISION OF VETERINARY MEDICINAL PRODUCTS
TITLE IV — THE EUROPEAN AGENCY FOR THE EVALUATION OF MEDICINAL PRODUCTS
TITLE V — GENERAL AND FINAL PROVISIONS
- ANNEX — PART A