|
|
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.
|
|
| Guidelines on active pharmaceutical ingredient master file procedure |
| Short Title: | Annex 4, WHO Technical Report Series 948, 2008 |
| Internet: | http://www.who.int/medicines/publications/pharmprep/OMS_TRS_948.pdf#page=113 |
| 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, Telegraph: UNISANTE GENEVA |
| Content: | These guidelines are intended to assist applicants in the compilation of the information on APIs in their dossiers for prequalification or when submitting a variation to a dossier on a prequalifi ed product (named in the text from
now on as product dossier) when the APIMF procedure is used. It is also intended to help APIMF holders in the compilation of their APIMFs. |
|
|
|
|
|
