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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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China’s NPMA (CFDA)

China’s NMPA (CFDA) – Webinar Recording/Transcript

$287.00
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01-22-20-Spreadsheet-Validation-Recording.png

Spreadsheet Validation – Webinar Recording/Transcript

$287.00
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Managing Data and Documentation for FDA Inspections

Managing Data and Documentation for FDA Inspections

$397.00
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Design Change Analysis

Design Change Analysis: Five Steps to Compliance

$397.00
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