Validation Under Good Laboratory Practices

Overview:
This webinar will discuss the best practices of analytical method
validation, including components of a validation, 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. 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 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]