Thursday, 11 April 2013

PDA CLEANING VALIDATION REPORT

Scope

The manufacture of modern pharmaceuticals is a complex process involving highly technical
personnel, complex equipment, sophisticated facilities and complicated processes. Individuals
responsible for all aspects of the production, approval and validation of products, such as quality
control, quality assurance, engineering, validation, production, research and development, contractors
and vendors and regulatory affairs personnel may use this document as a resource for establishing or
reviewing the cleaning programs within their facilities.

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