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Date Posted
News Title
2016/08/24
US: FDA statement on Medical Device User Fee Agreement (MDUFA)
2016/08/23
EU: EMA releases list of medical events for pharmacovigilance monitoring
2016/08/22
EU: Clinical trial delays prompt EMA to consider revising guidance
2016/08/19
Global: Making precision medicine work
2016/08/18
Global: 10 Disruptive Technologies and the Regulatory Implications
2016/08/17
Asia: Indias drug regulator allows concurrent applications for genetic-related trials
2016/08/16
US: FDA offers an updated policy on changes of capsule suppliers
2016/08/15
EU: Better monitoring of biological medicines
2016/08/12
EU: Data integrity - key to public health protection
2016/08/11
China: CFDA awards contract for development of regulatory data sharing platform
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