RE: Validation Master Plan Contribution from Carlos Nadal written on 12/28/2006 at 18:52
Original contribution: Validation Master Plan written by H. Martin on 3/21/2002 at 09:40) A Validation Master Plan is to provide an FDA or any auditor that you know all the systems in your facility that needs to be validated or revalidated. It should have specific dates responsibles people to accomplih the task. Once approved you can add or change providing a justification. Ussually a VMP can cover up to 5 years. For equipment in use it is include in the plan as a concurrent validation.
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