2021 Medical Device Industry Outlook
Read the results of our 2021 Medical Device Industry Outlook Survey, based on responses from 1600 professionals.
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WATCH NOW: Risk Management according to EN ISO 14971:2012
Since the publication of ISO 13485:2016, risk management is a major concern for maintaining regulatory compliance in major medical device markets.
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In Depth: 21 CFR Part 820 - FDA Quality System Regulation
Are you ready to sell your medical device in the United States? If so, your company must comply with the US FDA Quality System Regulation (QSR), sp
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