Safety pharmacology in pharmaceutical development approval and post marketing surveillance

"This book covers the regulatory required evaluation and study of the potentially adverse pharmacological effects of new drugs, from the general regulatory requirements to the specific studies that must be done and how they are performed and interpreted. Based on more than 30 years of direct ex...

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Bibliografische gegevens
Hoofdauteur: Gad, Shayne C. 1948-
Formaat: Boek
Taal:English
Gepubliceerd in: Boca Raton, FL CRC Press c2012.
Editie:2nd edition.
Onderwerpen: