MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

Webinar On Developing a Validation Master Plan

Event Details

Webinar On Developing a Validation Master Plan

Time: June 12, 2015 from 1pm to 2pm
Location: Online
Street: 5939 Candlebrook Ct
City/Town: Mississauga
Website or Map: https://compliancetrainings.c…
Phone: 4169154458
Event Type: webinar
Organized By: Compliance Trainings
Latest Activity: May 22, 2015

Export to Outlook or iCal (.ics)

Event Description

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



Project approach

Key activities

Project organization

Communication plan

Quality assurance

Who are the VMP Key contributors? Defining their roles

Quality Assurance

Regulatory Affairs



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

Price tags:


Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899


Single REC : For One Participant - Unlimited Access for 6 Months

$ 299


For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada 
Customer Support : #416-915-4458 
Email :

For more information about this event please visit

Comment Wall


RSVP for Webinar On Developing a Validation Master Plan to add comments!

Join MedTech I.Q.

Attending (1)

© 2020   Created by CC-Conrad Clyburn-MedForeSight.   Powered by

Badges  |  Report an Issue  |  Terms of Service