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, Qi Jiang, Li Zhu, Bin Yao
Format: Article
Language:English
Published: MDPI AG 2013-01-01
Series:Pharmaceutics
Subjects:
Online Access:http://www.mdpi.com/1999-4923/5/1/94