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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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| Multisource (generic) pharmaceutical products: guidelines on registration requirements |
| Short Title: | Annex 7, WHO Technical Report Series 937 |
| Internet: | http://whqlibdoc.who.int/trs/WHO_TRS_937_eng.pdf#page=359 |
| 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: | The guidance provides appropriate in vivo and in vitro requirements to assure interchangeability of the multisource product without compromising the safety, quality and efficacy of the pharmaceutical product. |
| Document Type: | Guide |
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