Developing a Validation Master Plan Webinar
This webinar will provide all medical device companies with a step by step process on how to develop a validation master 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.
Objectives of the Presentation:
This presentation aims at providing the participants a better insight on:
- What is a VMP and how is it valuable to my company?
- What topics are covered in the VMP and to what extent?
- How is the VMP controlled and updated?
- How is the VMP implemented?
- Who contributes to the VMP?