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Risk Management for Drug and Device Manufacturers: A Guide to FDA Policies and Processes, 2024 Edition
$397.00
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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Postmarket Surveillance in the Real World: The FDA’s Perspective on RWD/RWE – Webinar Recording/Transcript
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Inspection Readiness for EU GMP Annex 1 – Manufacture of Sterile Medicinal Products – Webinar Recording/Transcript
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FDA in 2024 and Beyond: What Election-Year Changes Mean for Your Business – Webinar Recording/Transcript
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FDA Oversight of Laboratory-Developed Tests — The Impact of the Final Rule – Webinar Recording/Transcript
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Managing Data and Documentation for FDA Inspections and Remote Assessments – Webinar Recording/Transcript
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Integrating Regulatory Intelligence into Supplier Management – Webinar Recording/Transcript
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