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QSR

Planning an Audit Response

Planning an Audit Response: How to Handle MDSAP Findings

$397.00
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Auditing for Quality Manufacturing

Auditing for Quality Manufacturing: Five Areas of Risk for Drug and Device Manufacturers

$397.00
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Medical Device Change Management

Medical Device Change Management – Webinar Recording/Transcript

$287.00
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FDA CDS Software Regulation

FDA CDS Software Regulation – Webinar Recording/Transcript

$287.00
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webinar recording

EU-MDR: Are You Ready? Part II – Webinar Recording/Transcript

$287.00
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Health Care Innovation and FDA Regulation

Healthcare Innovation and FDA Regulation – Webinar Recording/Transcript

$287.00
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Usability Engineering: How the Updated ISO 14971:2019 Changes Your Process

Usability Engineering: How the Updated ISO 14971:2019 Changes Your Process – Webinar Recording/Transcript

$287.00
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Top Customs and FDA Enforcement Issues for Imports of Pharmaceuticals, Biologics and Medical Devices

Top Customs and FDA Enforcement Issues for Imports of Pharmaceuticals, Biologics and Medical Devices – Webinar Recording/Transcript

$287.00
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How to Deploy Root Cause & CAPA to Minimize Human Error

How to Deploy Root Cause & CAPA to Minimize Human Error – Webinar Recording/Transcript

$287.00
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EU-MDR: Are You Ready? An Exclusive Three-Part FDAnews Webinar Series – Webinar Recording/Transcript

$646.00
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James Pink

EU-MDR: Are You Ready? Part I – Webinar Recording/Transcript

$287.00
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Effective Auditing for Manufacturing Quality webianr

Effective Auditing for Manufacturing Quality – Webinar Recording/Transcript

$287.00
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