This training will discuss regulatory requirements for monitoring of pharmaceutical impurities. It will explain how to monitor impurities in pharmaceutical products as per ICH Q3 A/B requirements and to measure the thresholds to report for regulatory submission.
Monitoring Impurities in Pharmaceutical Products - ICH Q3 requirements
16 January 2014, Palo Alto, United States
Introduction
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Online Event
Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States
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ComplianceOnline
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