Safety pharmacology in pharmaceutical development
approval and post marketing surveillance
by Shayne C. Gad
"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 experience, the author describes tricks and practical insights for making studies work and understanding why they don't. The second edition includes current regulations (US FDA and international especially Europe and Japan) and updated test methods, interpretation, and science"--Provided by publisher.
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Safety pharmacology in pharmaceutical development: approval and post marketing surveillance
2012, CRC Press/Taylor & Francis
in English
- 2nd ed.
1439845670 9781439845677
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Book Details
Edition Notes
Rev. ed. of: Safety pharmacology in pharmaceutical development and approval. c2004.
Includes bibliographical references and index.
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- Created March 23, 2012
- 6 revisions
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| December 20, 2022 | Edited by MARC Bot | import existing book |
| December 13, 2022 | Edited by MARC Bot | import existing book |
| October 17, 2020 | Edited by MARC Bot | import existing book |
| October 13, 2020 | Edited by ImportBot | import existing book |
| March 23, 2012 | Created by LC Bot | Imported from Library of Congress MARC record |