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Clinical Trials Adverse Event Reporting Guide - 2020 Edition
$397.00
Managing Data and Documentation for FDA Inspections - 2019
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Design Change Analysis: Five Steps to Compliance
$397.00
Winning Device EU Marketing Approval: Seven Steps to Writing Clinical Evaluation Reports
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$397.00
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From QSR to QMSR: Meeting FDA’s New Requirements
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ICH Q10 Pharmaceutical Quality System — Unpacked and Refreshed
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Risk Management for Drug and Device Manufacturers: A Guide to FDA Policies and Processes, 2024 Edition
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