PHARMACEUTICALS 2011 - How to transfer QC procedures for commercial products in pharma industry - ICH and USP guidelines - Pharmaceuticals webinar By ComplianceOnline

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Category Pharmaceuticals,conference,event,Webinar

Deadline: February 03, 2011 | Date: February 03, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2010-12-03 20:08:28 (GMT+9)

Call For Papers - CFP

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.

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.

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.