Validation Under Good Laboratory Practices 2017

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Category Good Laboratory Practices, Food and Drug Administration, fda calibration guidance, gxp documentation, medical device calibration, Compliance advanced Courses

Deadline: December 03, 2017 | Date: December 04, 2017

Venue/Country: Fremont, U.S.A

Updated: 2017-10-31 15:44:11 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com