Safety Monitoring in Clinical Trials

Monitoring patient safety during clinical trials is a critical component throughout the drug development life-cycle. Pharmaceutical sponsors must work proactively and collaboratively with all stakeholders to ensure a systematic approach to safety monitoring. The regulatory landscape has evolved with...

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Bibliographic Details
Main Authors: H. Amy Xia (Author), Qi Jiang (Author), Li Zhu (Author), Bin Yao (Author)
Format: Book
Published: MDPI AG, 2013-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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