Good Laboratory Practices - Under Analytical Method Validation

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Category Good Laboratory Practices, Validation Programs, Environmental Protection Agency, Lab Supervisors and Managers, laboratory management Courses, laboratory information system, Compliance Clinical Checklists, Online management courses

Deadline: September 11, 2017 | Date: September 12, 2017

Venue/Country: Fremont, U.S.A

Updated: 2017-07-17 15:59:14 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com