| dc.contributor.author | Edited by Huynh-Ba, Kim | |
| dc.date.accessioned | 2020-08-26T08:54:23Z | |
| dc.date.available | 2020-08-26T08:54:23Z | |
| dc.date.issued | 2009 | |
| dc.identifier.citation | Huynh-Ba, Kim (2009). Handbook of stability testing in pharmaceutical development: regulations, methodologies, and best practices. New York : Springer. | en_US |
| dc.identifier.isbn | 978-0-387-85626-1 | |
| dc.identifier.uri | http://hdl.handle.net/123456789/1365 | |
| dc.description.abstract | This handbook is the first to cover all aspects of stability testing in pharmaceutical development. Written by a group of international experts, the book presents a scientific understanding of regulations and balances methodologies and best practices. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Springer | en_US |
| dc.subject | Drug stability | en_US |
| dc.subject | Drugs - testing | en_US |
| dc.subject | Drug development | en_US |
| dc.title | Handbook of stability testing in pharmaceutical development: regulations, methodologies, and best practices | en_US |
| dc.type | Book | en_US |
