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Good Laboratory Practices - Under Analytical Method Validation

Event Details

Good Laboratory Practices - Under Analytical Method Validation

Time: September 12, 2017 from 10am to 11am
Location: Online
Street: 161 Mission Falls Lane, Suite 216
City/Town: Fremont
Website or Map: http://www.compliance4all.com…
Phone: 08004479407
Event Type: webinar
Organized By: Adam Fleming
Latest Activity: Jul 17, 2017

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Event Description

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

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