Introduction

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.

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Venue

Online Event

Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States

Organised by

ComplianceOnline

Contact information

Mr admin
Palo Alto, 94303, United States of America
650-620-3915
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