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The CenterWatch Weekly, August 21, 2017

08:00 EDT 21 Aug 2017 | CentreWatch

New EU medical device regulations cause industry shake up Medical device manufacturers will need to provide substantially more clinical evidence to support claims of safety and performance for many medical and in vitro diagnostic (IVD) devices marketed in the European Union (EU) as the result of two new regulations adopted by the European Parliament. The […]

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Original Article: The CenterWatch Weekly, August 21, 2017

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