This laboratory compliance training will teach you how to validate an analytical method under the GLP requirements. It will cover in detail the criteria for the validation of an analytical method including statistical and documentation requirements.
This webinar will teach you how to validate an analytical method under the GLP requirements.
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. All methods must be validated. Common criteria are accuracy, precision, linearity, range, and several more.This webinar will teach you how to validate an analytical method under the GLP requirements.
Areas Covered in the Webinar:
- Method validation
- The criteria for a method
- Statistical requirements
- Documentation requirements
- Common issues
Who Will Benefit:
This webinar will provide valuable assistance to all personnel working in a GLP certified laboratory and for those developing methods for environmental analysis, chemicals, petroleum products and petrochemicals. Employees who will benefit include:- QA Managers
- QC Managers
- Analytical Chemists
- Validation Specialists
- Laboratory Managers and Supervisors
- Regulatory Affairs Personnel
- Documentation Specialists
Course Provider
John Fetzer,
