2 Day Virtual Medical Device Studies Training Course: Regulatory Requirements and Adverse Event Reporting ...Middle East

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2 Day Virtual Medical Device Studies Training Course: Regulatory Requirements and Adverse Event Reporting
DUBLIN, Nov. 27, 2023 /PRNewswire/ -- The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course" conference has been added to ResearchAndMarkets.com's offering. This seminar provides an essential overview of medical device clinical evaluations,...

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