This snapshot, taken on 02/08/2006, shows web content selected for preservation by The National Archives. External links, forms and search boxes may not work in archived websites.
EudraLex
|
|
| Pharmaceuticals > EudraLex | |
| Volume 1 - Pharmaceutical Legislation. Medicinal Products for Human use. |
|
| Volume 2 - Notice to Applicants. Medicinal Products for Human use. |
|
| Volume 3 - Guidelines. Medicinal Products for Human use. |
|
| Volume 4 - Good Manufacturing Practices Medicinal Products for Human and Veterinary use. |
|
| Volume 5 - Pharmaceutical Legislation. Veterinary Medicinal Products. |
|
| Volume 6 - Notice to Applicants. Veterinary Medicinal Products. |
|
| Volume 7 - Guidelines. Veterinary Medicinal Products. |
|
| Volume 8 - Maximum residue limits. Veterinary Medicinal Products. |
|
| Volume 9 - Pharmacovigilance Medicinal Products for Human and Veterinary use. |
|
| Pharmaceuticals legislation on CD | |
| Miscellaneous : Guidelines
on Good Distribution Practice of Medicinal Products for Human Use
(94/C 63/03) These guidelines have been prepared in accordance with Article 10 of Council Directive 92/25/EEC of 31 March 1992 on the wholesale distribution of medicinal products for human use . They do not cover commercial relationships between parties involved in distribution of medicinal products nor questions of safety at work. |
|
|
European Commission - Enterprise and Industry Directorate General - Consumer goods - Pharmaceuticals - Last update :