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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.
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| WHO Supplementary Guideline on Good Manufacturing Practices: Validation |
| Short Title: | Annex 4, WHO Technical Report Series 937 |
| Internet: | http://www.who.int/medicines/publications/pharmprep/TRS_937.pdf#page=119 |
| Origin/Publisher: | WHO headquarters, Avenue Appia 20, 1211 Geneva 27, Switzerland, Telephone: (+ 41 22) 791 21 11, Facsimile (fax): (+ 41 22) 791 3111, Telex: 415 416, www.who.int |
| Content: | Guideline with focus on the overall concept of validation (API and Medicinal Products) |
| Document Type: | Guide |
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