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Online Webinar
03 Feb 2011

Webinar On ICH and USP guidelines

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.

Why Should You Attend:Once a product goes commercial, measuring the quality, safety, and efficacy attributes of the drug substance and the drug product is crucial. There are well-established ICH guidelines for the validation requirements of typical analytical procedures. In contrast, the requirements for a technical transfer of an analytical procedure from one site to another or within a site to a separate facility are often debated.Areas Covered in the Seminar:ICH guidelines for validation.USP guidelines for validation and verification.Applications of the ICH guidelines for method transfer.Debated topics and approaches.Complex procedures.Establishing boundaries. 


3 Feb 2011 @ 10:00 am

3 Feb 2011 @ 11:30 am

Duration: 1 hours, 30 minutes



Online Webinar


English en

Organised by

ComplianceOnline (deactivated)

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