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Risk Management for Drug and Device Manufacturers: A Guide to FDA Policies and Processes, 2024 Edition
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A foundational volume for manufacturers and the consultants that serve them, FDAnews’ Risk Management for Drug and Device Manufacturers: A Guide to FDA Policies and Processes, 2024 Edition has all the references you need in one handy volume.
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Latest Medical Device Postmarket Surveillance Requirements from China’s NMPA and the U.S. FDA – Webinar Recording/Transcript
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Data Integrity for Drug and Device Manufacturers: Avoiding Breaches and Closing Gaps
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Data Integrity in the COVID-19 Era and Beyond — Part III: The Real-World Costs of Data Integrity – Virtual Conference Recording/Transcript
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