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How To Build Quality Into Commissioning And Validation
This webinar will provide valuable assistance to all regulated companies that need to commission and validate their systems, including companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields.
Description
Learn how to complete yours from a Principal Consultant with 20 years of experience and numerous letters of recommendation for bringing commissioning and validation projects in on time and on budget.
This seminar uses real-life examples to identify and explain the 5 keys to building quality into commissioning and validation projects. The seminar also illustrates ways to quantify these 5 keys so that different options can be compared and optimal solutions (for performing commissioning and validation) identified. Many commissioning and validation projects exceed their allocated time and/or budget.
Areas Covered in the seminar:
- Introduction - Example 1: (Real-Life Validation Situation).
- Highly Talented People.
- 8 Points To Consider And How to Evaluate Them.
- Proper Planning.
- Example 2
- 10 Issues You’ll Face and How To Deal With Them.
- Good Design
- How An Iterative Approach Accomplishes This.
- Leverage
- Buy-In
- 3 Aspects of "Buy-in" that are critical (and how to get them)
Who will benefit:
This webinar will provide valuable assistance to all regulated companies that need to commission and validate their systems, including companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:
- Principals and Executives of Pharmaceutical, Biotechnology, and Medical Device Firms
- End-users responsible for systems that need to be validated
- QA Managers and personnel
- Information Technology Managers and personnel
- Validation Specialists
- Process Engineering Managers and personnel
- Consultants
Instructor Profile:
Jeffery Gassman, has 20 years of commissioning and validation experience for biotechnology and pharmaceutical clients nationally and internationally. He earned his B.S. in Chemical Engineering from Clarkson University, and his M.S. in Chemical Engineering from Columbia University. In 1995, he became the President of Validation Plus (VPI). His work and leadership has been instrumental in VPI receiving numerous letters of recommendation. Mr. Gassman is a Dale Carnegie graduate, and was elected (in 2004) to Who’s Who in Science and Engineering in America.
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