Developing a Validation Master Plan - By Compliance Global Inc.

Developing a Validation Master Plan - By Compliance Global Inc.

 

  • Developing a Validation Master Plan By Compliance Global Inc

    Live Session for one participant

    Sale Date Ended

    USD 155
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About The Event

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/MariaDorat/developing-a-validation-master-plan/1


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