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Content tagged with Clinical Evaluation Report

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Let's Get you Ready for your Clinical Trial | Webinar | EU perspective

Whether you are a first-time inventor or a large manufacturer, the thrill of bringing a medical device to market is both exhilarating and overwhelming. The development of a successful device not only requires optimized design efforts, but also clinical, regulatory & marketing expertise. Download this 30 min. webinar and increase your chances of successfully launching your medical device.


By when do I need to update the Clinical Evaluation Report?

By when do I need to update the Clinical Evaluation Report?


KPMG, RAPS survey finds many device makers ill-prepared for 2020’s EU MDR

An industry survey conducted by KPMG and the Regulatory Affairs Professionals Society (RAPS) found little familiarity with the European Union’s new Medical Device Regulation and its requirements that take full effect in May 2020.