Master Validation Plan - A Complete Package Webinar
Time: 11:30 AM PST, 02:30 PM EST
Duration: 90 Minutes
Instructor: Marie Dorat
This course will provide guidance on best practices for developing and implementing a good plan detailing responsibilities and deliverables to make validation efficient and consistent. It will provide a step-by-step guidance for medical device companies that need to develop a validation master plan (VMP) for product/equipment transfer, facilities, processes or to develop a company standard.
Why Should you Attend
The Validation Master Plan webinar describes the way an organization may approach validation; help identify 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:
- 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?