The rules governing medicinal products in the European Union
| Μορφή: | Βιβλίο |
|---|---|
| Γλώσσα: | English |
| Στοιχεία έκδοσης: |
Luxembourg :
Office for Official Publications of the European Communities,
1998-1999
|
| Ταξινομικός αριθμός: |
KET 362.1 RUL |
| Θέματα: | |
| Ετικέτες: |
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Πίνακας περιεχομένων:
- 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