Analytical Instrument 2015 - Webinar on Analytical Instrument Qualification According The New Revision of USP 1058

Overview:
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:
Scope and principles of the new revision.
Changes to the existing chapter
Approaches for risk based qualification
The 4Q Qualification lifecycle approach: DQ, IQ, OQ, PQ
Purpose and contents of qualification phases: DQ, IQ, OQ, PQ
Dealing with three instrument categories A, B and C
Procedures and validation deliverables for the three categories
The importance of the quality agreement between users and suppliers
Integrating software validation and equipment qualification
Integrating the USP 1058 revision with the GAMP Guide on Laboratory Computerized Systems
Dealing with changes of software, firmware and equipment hardware
Recommendations for effective implementation of the new revision
For Easy Implementation, Attendees Will Receive:
Analytical Instrument Qualification for <1058>
Allocating Analytical Instruments to USP <1058> categories
Procedures and deliverables for USP <1058> categories
Who Will Benefit:
QC managers
QA managers and personnel
Analysts and lab managers
QA managers and personnel
Regulatory affairs
Training departments
Documentation department
Consultans
Speaker Profile:
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
Contact Detail:
NetZealous - Compliance4All,
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539, USA.
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com
http://www.compliance4all.com/
Event Link : http://bit.ly/1L4WgHV