Marketing authorization of pharmaceutical products with special reference to multisource (generic) products : a manual for National Medicines Regulatory Authorities (NMRAs)
Publication details: Geneva : WHO, 2011.Description: 148 pageContent type:- text
- unmediated
- volume
- 9789241501453
Hello from Record Display Customizations!
| Cover image | Item type | Current library | Home library | Collection | Shelving location | Call number | Materials specified | Vol info | URL | Copy number | Status | Notes | Date due | Barcode | Item holds | Item hold queue priority | Course reserves | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Book
|
DOH Central Library WHO Publication Section | QV 33 MAR 2011 (Browse shelf(Opens below)) | Available | D0001B000047 |
Browsing DOH Central Library shelves,Shelving location: WHO Publication Section Close shelf browser (Hides shelf browser)
| QV 16 BIO 1987 Biological substances : international standards and reference reagents : 1990 | QV 21.88 ETH 1988 Ethical criteria for medicinal drug promotion | QV 33 EFF 2002 Effective drug regulation : | QV 33 MAR 2011 Marketing authorization of pharmaceutical products with special reference to multisource (generic) products : | QV 33 QUA 1997 Quality assurance of pharmaceuticals : | QV 33 QUA 1999 Quality assurance of pharmaceuticals : | QV 33 QUA 2004 Quality assurance of pharmaceuticals : |
There are no comments on this title.
Log in to your account to post a comment.