Generic Drug Product Development : International Regulatory Requirements for Bioequivalence : : Drug and Pharmaceutical Sciences Vol - 201Textual Documents
Kanfer, Isadore.
Generic Drug Product Development : International Regulatory Requirements for Bioequivalence : : Drug and Pharmaceutical Sciences Vol - 201 Textual Documents
- 1st ed.
- London Informa Healthcare 2010
- 309.
9780849377853
Pharmaceutics(Manufacture & Preparation)
615.191 / KAN
Generic Drug Product Development : International Regulatory Requirements for Bioequivalence : : Drug and Pharmaceutical Sciences Vol - 201
APA
Kanfer I., Shargel L., . (2010). Generic Drug Product Development : International Regulatory Requirements for Bioequivalence : : Drug and Pharmaceutical Sciences Vol - 201. London: Informa Healthcare.
Chicago
Kanfer Isadore, Shargel Leon, . 2010. Generic Drug Product Development : International Regulatory Requirements for Bioequivalence : : Drug and Pharmaceutical Sciences Vol - 201. London: Informa Healthcare.
Harvard
Kanfer I., Shargel L., . (2010). Generic Drug Product Development : International Regulatory Requirements for Bioequivalence : : Drug and Pharmaceutical Sciences Vol - 201. London: Informa Healthcare.
MLA
Kanfer Isadore, Shargel Leon, . Generic Drug Product Development : International Regulatory Requirements for Bioequivalence : : Drug and Pharmaceutical Sciences Vol - 201. London: Informa Healthcare. 2010.
