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This edition of Fundamentals of EU Regulatory Affairs focuses on changes to healthcare product development, manufacturing and marketing across the EU. The most significant changes since the introduction of the Medical Devices Directive are coming with the implementation of the EU Medical Device Regulation and EU In Vitro Diagnostic Device Regulation. Clinical trial regulations implementation has been delayed, but its impact is discussed. There are several new chapters in this edition, covering EMA and other EU regulatory bodies, preparing for EMA meetings, regulatory strategy, medical device preclinical testing, adaptive and alternative medicinal product pathways and more. This book is an excellent reference for anyone at any level working in regulatory affairs in the EU market and a useful tool for those planning to sit for the RAC (EU) exam.
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