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This webinar will provide all medical device companies with a step by step process on how to develop a master validation plan (VMP) for product/equipment transfer, facilities, or to develop a company standard. It will also provide a detailed insight on the best practices for developing and implementing a good plan detailing responsibilities, and deliverables to make validation efficient, and consistent.
Why Should You Attend
Attend this webinar to learn in detail how to develop a VMP and what are the best methods to be followed. The Validation Master Plan describes the way an organization approaches validation; who controls the various aspects of the validation activities; and how production, quality and management will be involved. The VMP also details the validation requirements for each test/ system/ equipment and will guide the organization in achieving its objectives.
Areas Covered in this Webinar
This webinar aims at providing the participants a better insight on:
How to develop and implement a Validation Master Plan
Who Will Benefit
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