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Date: 17th June, 2008

Location: Web seminar, USA

Summary:
Pharmaceutical - Training, Seminar

A Validation Master Plan is not a mandatory document, but is usually one of the key documents an auditor will ask to review. It is a document that dictates the way a company approaches validation, identifying who has control over the various aspects of the validation activities, and how production, quality, and management will be involved. The VMP also establishes the validation requirements for each test/system/equipment and will guide the organization in achieving its objectives.

This live and comprehensive web seminar will provide an introduction to the creation, implementation and maintenance of Validation Master Plans.

Key Discussion Points will include:
What is a VMP?
Why is a VMP valuable to my company?
What is defined in the VMP?
How is the VMP controlled and updated?
How is the VMP implemented?
Who contributes to the VMP?

Learning Benefits: Upon completion of this course, participants will have a better understanding of:
Identifying the validation concerns for your company
Identifying the validation requirements for your company
Establishing a written plan
Taking a holistic approach to validation
Achieving synergy among validation programs
Providing clear guidance to your organization