Laboratory Compliance 2012 - Validation of Analytical Procedures for Use in the Pharmaceutical Industry

This 6-hr virtual seminar will review analytical procedures used in assessing quality, safety and efficacy of drug products. It will cover the ICH and USP guidelines for procedure validation and help you ensure robust validation of analytical procedures for drug substances and products.

This 6-hr training will examine the analytical tools used throughout a drug product life cycle. There is a broad range of assays and techniques used to measure the quality, safety and efficacy of a drug substance or a drug product. The training will challenge attendees to give thoughtful evaluation of their current strategies or to develop strategies from the ground up. The CFR regulations and guidance from the USP and ICH will be used as references and in support of creating a sound approach to the validation of analytical procedures for drug substances and products.