Aug 13, 2018 | 10:00 AM | Monday
This analytical method validation webinar will provide practical tips on how to validate an analytical method under the GLP requirements.
Start on : August 13, 2018 10:00 AM Monday
End on : August 13, 2018 11:00 AM Monday
This webinar will discuss the best practices of analytical method validation, including components of a validation, how to include critical reagents comparison, selectivity experiments, assessment of stability, importance of communication between the development and the validation labs and accuracy of transfer documents.
Why should you Attend:
Any laboratory that supports products for sale or use in the United States must follow Good Laboratory Practices (GLP), a comprehensive system that guarantees validity of results. If you work in pharmaceuticals, chemicals and petrochemicals, and environmental analyses then you are mandated to be following GLP. One of the major tasks in GLP is validation of an analytical method.
Areas Covered in the Session:
The Criteria for a Method
Who Will Benefit:
Lab Supervisors and Managers
QA Managers and Personnel
John C. Fetzer has had over 30 year experience in HPLC methods development. He has authored or co-authored over 50 peer-reviewed papers onl iquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and Bioanalytical Chemistry.
Event Fee: One Dial-in One Attendee Price: US $150.00
Compliance4All DBA NetZealous,
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