161 Mission Falls Lane, Suite 216,

Fremont,

CA,

US,

ZIP: 94539

Phone: 18004479407

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: [email protected]