It is critical that a robust transfer program be put into place in order to head off issues. Unearthing issues at the drug development stage, rather than during routine manufacture, will improve the overall success of the project. Attend this webinar to understand the ICH and USP guidance for validation, and how to apply ICH guidelines for method transfer and how to establish boundaries.
How to transfer QC procedures for commercial products in pharma industry - ICH and USP guidelines - Webinar By ComplianceOnline
3 February 2011, Palo Alto, United States
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Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States
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ComplianceOnline
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