The rules governing medicinal products in the European Union (Luxembourg : Office for Official Publications of the European Communities, 1998)
V.1 Pharmaceutical legislation. Medical products for human use -- v.2a. Notice to applicants. Medicinal products for human use. Procedures for marketing authorisation -- v.2b. Notice to applicants. Medicinal products for human use. Presentation and content of the dossier -- v. 3a. Guidelines : medicinal products for human use : quality and biotechnology -- v. 3b. Guidelines : medicinal products for human use : safety, environment and information -- v. 3c. Guidelines : medicinal products for human use : efficacy -- v. 4. Pharmaceutical legislation : medicinal products for human and veterinary use : good manufacturing practices -- v.5. Pharmaceutical legislation. Veterinary medicinal products -- v. 6a. Notice to applicants. Veterinary medicinal products. Procedures for marketing authorisation -- v.6b. Notice to applicants. Veterinary medicinal products. Presentation and content of the dossier -- V.7a. Guidelines, veterinary medicinal products : General, efficacy, environmental risk assessment -- v.7b. Guidelines: veterinary medicinal products : immunologicals, quality
Keywords: Drugs -- Law and legislation -- European Union countries