Webinars Details - How to Minimize Costs and still ensure Compliance while Validating Manufacturing Systems
Webinars
Event
- Title:
- How to Minimize Costs and still ensure Compliance while Validating Manufacturing Systems
- When:
- 04.27.2010
- Category:
- Manufacturing
Description
Webinar Date: April 27, 2010 Time: 12:00 to 12:30 PST
Summary:
Validation is sometimes considered an ugly word in Engineering or Manufacturing departments, where technical staff are used to onerous non-value added documentation work associated with validation. Validation is an essential and important part of the Manufacturing process and should be a high-value exercise when done right.
Join our discussion on April 27, 2010 to review Risk Based approaches to validation. Our USDM Subject Matter Expert will present multiple case studies for Manufacturing systems validation. The key highlights of the webinar include:
- What is a risk based approach to validation? Case Studies and examples will be presented.
- How to conduct effective risk assessments and what are the different risk assessment techniques?
- How to use the risk assessment as a stepping stone to more effective test protocols?
- How to design high quality and efficient test scripts?
- How to prevent attachment overkill? How to ensure only high value objective evidence is obtained?
- Use of other tools and tips to speed up the validation effort.
Discover and discuss this topic with the USDM experts and your peers in the industry!
Sponsored By: USDM's Manufacturing Practice Learn More
Visit our website to register for additional Manufacturing Practice Webinars
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About USDM
USDM is a leading global consulting firm focused on life sciences. We specialize in regulated business processes, with an emphasis on compliance and performance.
USDM provides innovative services and solutions that enable life science companies to achieve and maintain compliance across the entire enterprise.
