Online Training 2015 - Developing a Validation Master Plan - By Compliance Global Inc

Overview
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:
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?
Learning Objectives
How to develop and implement a Validation Master Plan
Who Will Benefit
Quality Assurance Personnel
Regulatory Affairs Professionals
Operations Staff
Engineers
Quality Engineers
Level
Beginner
For more detail please click on this below link:
https://complianceglobal.us/product/700254/MariaDo...
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