|
|
The following guideline can be ordered through the address listed in the "Source/Publisher"-category.
In cases in which you can order through the Internet we have established a hyperlink.
|
|
| Good Manufacturing Practices for Pharmaceutical Products (in WHO Technical Report Series 823, 1992) |
| Origin/Publisher: | World Health Organisation (WHO), Distribution and Sales, Post Box, CH - 1211 Geneva 27 |
| Content: | GMP rules of the World Health Organisation which have become part of German legislation via the Pharmabetriebsverordnung (operation ordinance for pharmaceutical entrepreneurs). Frequently a foundation for the manufacture and testing of medicinal products in the Third World. |
| Document Type: | WHO Technical Report |
|
|
|
|
|
