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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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FDA Oversight of Laboratory-Developed Tests — The Impact of the Final Rule
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A Masterclass on Effective 483 Response
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Best Practices for Clinical Trial Site Management, Vol. 4
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