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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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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
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Create a Quality Culture to Aid Risk Management: Dynamic Behaviors that Achieve Quality and Business Objectives – Webinar Recording/Transcript
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FDA’s Plan to Modernize the 510(k) Pathway: What Regulatory, Quality and Compliance Professionals Need to Know – 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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CDRH’s New Accreditation Scheme for Conformity Assessment: Impacts on Your Future Testing Plans and FDA Submissions – Webinar Recording/Transcript
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FDA Digital Health Regulation: Latest Developments for Medical Device Manufacturers – Webinar Recording/Transcript
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