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Post-Market Activities in the EU-MDR — A Detailed Analysis

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Category Quality Assurance, Regulatory Affairs

Deadline: January 30, 2020 | Date: January 30, 2020

Venue/Country: Online Webinar, U.S.A

Updated: 2020-01-04 17:37:43 (GMT+9)

Call For Papers - CFP

Recently, the European Union has revised the regulatory requirements governing medical devices; including the establishment of new expectations and approaches to post-market surveillance. Mandatory compliance to the new European Medical Device Regulation (MDR) is set for 26 May 2020.

Session Highlights:

Topic 1: Benefits of Post-Market Surveillance

Topic 2: Review the new EU-MDR 2017/745

Topic 3: Risk Management


Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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