2015 - Webinar On Developing a Validation Master Plan

Description :
This course 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.
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. 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 the Session :
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?
Overview of Validation Master Plan
What is a VMP?
Which regulations apply?
What topics are covered in the VMP?
Master Validation Plan content
Purpose
Scope
Project approach
Key activities
Project organization
Communication plan
Quality assurance
Who are the VMP Key contributors? Defining their roles
Quality Assurance
Regulatory Affairs
Operations
Engineering
Implementation of the VMP
Training requirements
Controlling and updating the VMP
Who Will Benefit:
Quality Assurance Teams
Regulatory affairs Teams
Operations Teams
Engineers Teams
Quality Engineers Teams
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support-AT-compliancetrainings.com