Validation Master Plan
KS441QL6L4CP1B16JCKL
A Validation Master Plan, also referred to as "VMP", outlines the principles involved in the qualification of a facility, defining the areas and systems to be validated, and provides a written program for achieving and maintaining a qualified facility. A VMP is the foundation for the validation program and should include process validation, facility and utility qualification and validation, equipment qualification, cleaning and computer validation. It is a key document in the GMP regulated pharmaceutical industry as it drives a structured approach to validation projects.
Read more on WikipediaHave feedback on this skill? Let us know.