Analytical Method Development and Validation

Venue: Radisson SAS Hotel

Location: Dublin, Ireland

Event Date/Time: May 14, 2009 End Date/Time: May 14, 2009
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Description

Analytical methods must be validated to provide reliable data for regulatory submissions. These methods are essential for a number of purposes, including testing for QC release, testing of stability samples, testing of reference materials and to provide data to support specifications.
This course provides a comprehensive coverage of the method development and validation requirements that are essential to progress a pharmaceutical compound, at each stage of product development. Upon completion of this course, delegates will have learned what is necessary to develop and validate methods for drug substance and drug product to comply with international regulatory guidelines.

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