ComplianceOnline

How To Build Quality Into Commissioning And Validation

Instructor: Jeffery Gassman
Product ID: 700888
  • Duration: 60 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

$500.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-963-2556

Email: customercare@complianceonline.com

Read Frequently Asked Questions

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
    • 6 Ways To 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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