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FDA’s Plan for Modernizing the 510(k) Pathway - Webinar Recording/Transcript

$287.00
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FDA Medical Device Compliance and Enforcement - Webinar Recording/Transcript

$287.00
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Regulating Software Used by Life Science Manufacturers - Webinar Recording/Transcript

$287.00
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Sampling Plans for Quality Audits - Webinar Recording/Transcript

$287.00
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Medical Device Voluntary Malfunction Disclosure Regulation - Webinar Recording/Transcript

$287.00
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Medical Device Cybersecurity Risks & Best Practices - Webinar Recording/Transcript

$287.00
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Laboratory Developed Tests, In Vitro Diagnostics & Gene Therapies - Webinar Recording/ Transcript

$287.00
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The 510(k) Process - Webinar Recording/Transcript

$287.00
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Brexit and the Impact to Your Global Business Operations - Webinar Recording/Transcript

$287.00
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Device Software Development: A Guide to Risk Management Requirements

Device Software Development: A Guide to Risk Management Requirements

$397.00
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Understanding ISO 19011:2018 - Webinar Recording/Transcript

$287.00
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Medical Device Software and Risk Management - Webinar Recording/Transcript

$287.00
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