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Good Laboratory Practices - Under Analytical Method Validation


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Who should attend?

QA Managers and Personnel Consultants Validation Specialists Chemists

Details

Overview:
All methods must be validated, the proof that they do what is claimed. Common criteria are accuracy, precision, linearity, range, and several more.

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:
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 on liquid chromatography, has served on the editorial advisory boards of the Journal of Chromatography, Analytical Chemistry, and Analytical and 
Bioanalytical Chemistry.

Event Cost & Details:
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=501439LIVE?channel=pharmiweb_Sep_2017_SEO

Prices

One Dial-in One Attendee Price: US$150.00

Contact

Event Manager
support@compliance4all.com

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