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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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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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Medical Device Regulatory Policy: Breakthrough Technologies, STeP and — Wait for It — Reimbursement – Webinar Recording/Transcript
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Spreadsheet Validation: Best Practices to Maintain Compliance – Webinar Recording/Transcript
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On-Site Inspections: They’re Back — But When, Where and How – Webinar Recording/Transcript
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The Biden Administration’s FDA: The First Six Months and What to Expect for the Rest of the Year – Webinar Recording/Transcript
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Demystifying AI in the Life Sciences Industry: What Regulatory, Quality and Compliance Professionals Need to Know – Webinar Recording/Transcript
$287.00