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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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FDA Medical Device Inspections in the Postpandemic World: Are You Ready for New Approaches and Methods? – Webinar Recording/Transcript
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Designing Secure Medical Devices: Building Cybersecurity into the Development Process
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Statistics and Data for Regulatory Professionals and Attorneys: Product Performance Evidence Made Easy – Webinar Recording/Transcript
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Quality Culture at the Crossroads: Building a Culture of Quality for Increased Success – Webinar Recording/Transcript
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The Biden Administration’s FDA: A Remarkable 2021, What to Expect in 2022 – Webinar Recording/Transcript
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Medical Device Premarket Review Pathways and FDA Mechanisms for Expedited Review – Webinar Recording/Transcript
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Promoting & Marketing in the Digital and Virtual World – Webinar Recording/Transcript
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