Validation Under Good Laboratory Practices 2017
It is recommended for laboratories that are under, or want to be under, GLP.
Sun, Dec 3, 2017 10:00 AM (PST)
Online,
Fremont,
California
Questions? Contact Event Organizer
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Sun, Dec 03 - 11:00 AM
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Overview:
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.
Areas Covered in the Session:
Method Validation
The Criteria for a Method
Statistical Requirements
Maintaining Compliance
Who Will Benefit:
Analysts
Lab Supervisors and Managers
QA Managers and Personnel
Consultants
Validation Specialists
Chemists
Speaker Profile:
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
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501596LIVE?channel=ticketprinting_Dec_2017_SEO
Full Details & Registration Link:
http://www.compliance4all.com/control/w_product/~product_id=501596LIVE?channel=ticketprinting_Dec_2017_SEO
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