Webinars
Event
- Title:
- Commissioning Vs. Validation
- When:
- 07.21.2010
- Category:
- Manufacturing
Description
Webinar Date: July 21, 2010 Time: 11:00 to 11:30 PST
Summary:
Within a life science manufacturing facility, there are several facility, utility, packaging and manufacturing systems with varying degrees of criticality. Furthermore, most systems are developed by established vendors who perform extensive vendor internal testing.
Join us on Wednesday, July 21, 2010 for a webinar to discuss how to leverage a commissioning approach to your manufacturing systems and equipment. The key highlights of the webinar include:
- What is commissioning? How is it different from Validation?
- Discuss the deliverables of commissioning and validation.
- The importance of a Validation Plan and a Risk Assessment.
- The importance of conducting a thorough Vendor Assessment.
- How to leverage FATs, SATs, Vendor Assessments and Vendor Testing in the validation / commissioning 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.
