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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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Impact of Artificial Intelligence and New Technology on Device Regulatory Compliance – Webinar Recording/Transcript
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Medical Device Cybersecurity: The Regulatory Landscape and How to Defend Your Practices During an Inspection – Webinar Recording/Transcript
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The Inextricable Link Between Data Integrity and Quality Culture – Webinar Recording/Transcript
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Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success – Webinar Recording/Transcript
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Manufacturing Quality: Using Audit Observations to Predict Problems – Webinar Recording/Transcript
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FDA Pathways to Bring your Medical Device to Market: What Regulatory Professionals Need to Know – Webinar Recording/Transcript
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