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Nonclinical Safety Assessment : a Guide to International Pharmaceutical Regulations.
Bringing a new drug to market is a costly time-consuming process. Increased regional and international regulation over the last twenty years, while necessary, has only served to amplify these costs. In response to this escalation, developmental strategies have shifted towards a more global approach....
| Clasificación: | Libro Electrónico |
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| Autor principal: | |
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Hoboken :
Wiley,
2013.
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| Temas: | |
| Acceso en línea: | Texto completo |
| Sumario: | Bringing a new drug to market is a costly time-consuming process. Increased regional and international regulation over the last twenty years, while necessary, has only served to amplify these costs. In response to this escalation, developmental strategies have shifted towards a more global approach. In order to create the most cost-effective and safe processes, it is critical for those bringing drugs to market to understand both the globally accepted regulations and the local variations. Nonclinical Safety Assessment: A Guide to International Pharmaceutical Regulations provides a. |
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| Notas: | 6.3.2 Risk Mitigation in Nonclinical Development of Medicinal Products. |
| Descripción Física: | 1 online resource (487 pages) |
| Bibliografía: | Includes bibliographical references and index. |
| ISBN: | 9781118517017 1118517016 9781118516980 1118516982 9780470745915 0470745916 |