The first version of USP <1058> has been released in 2008. Since then it has evolved as the global standard for analytical instrument qualification, despite of some deficiencies of the first version.
For example, the industry had difficulties to apply the chapter for systems comprising equipment hardware and computer systems. In addition, there have always been comments about not enough details for the four qualification phases. These deficiencies have been clarified in the new revision with much more details on integrated systems but still some interpretation is required for compliant and efficient implementation. This webinar will discuss all details and give strategies and case studies for easy implementation.
Areas Covered in the Session:
For Easy Implementation, Attendees Will Receive:
Who Will Benefit:
Ludwig Huber Ph.D., is the director and editor of Labcompliance the global online resource for validation and compliance. He is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems, Informa Healthcare". He has given more than 300 presentations mainly on GLP/GMP, 21 CFR Part 11 and Validation around the world. For more information, please visit Dr. Huber’s website www.ludwig-huber.com
NetZealous - Compliance4All,
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Fremont, CA 94539, USA.
Event Link : http://bit.ly/1L4WgHV