Validation and Qualification in the Regulated Environment
27 October 2016

This white paper gives an overview of validation and qualification in a GMP (Good Manufacturing Practice) environment. It goes onto describe the four stages (DQ, IQ, OQ and PQ) of the qualification procedure in detail and explains their context within the drug development lifecycle. Validation can be a cost intensive process but it is essential to ensure product quality and avoid product recalls. 

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