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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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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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Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript
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Maintaining Your Risk-Based Cleaning and Disinfectant Programs: Best Practices During COVID-19 – Webinar Recording/Transcript
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Digital Health Regulation: Navigating FDA’s Rules for Software as a Medical Device
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The MDSAP Audit Process: Latest Developments and Best Practices – Webinar Recording/Transcript
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Consumer Diagnostics and Wellness Testing: Navigating the Medical Device Regulations – Webinar Recording/Transcript
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Medical Device Cybersecurity: Understand the Latest Developments – Webinar Recording/Transcript
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CDRH’s Proposed Rule Harmonizing QSR and ISO 13485: Everything Devicemakers Must Know and Do to Prepare – Webinar Recording/Transcript
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