Monitoring Impurities in Pharmaceutical Products - ICH Q3 requirements

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.

04 de marzo de 2015 | Palo Alto (Estados Unidos)

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Online Event

2600 E. Bayshore Road

Palo Alto (Estados Unidos)

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ComplianceOnline

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