Good Laboratory Practice Regulations - Introduction and Strategies for Implementation 2016 is a webinar that covers topics such as:
- Objectives and concepts of GLP`s
- FDA and International GLP regulations: 21 CFR Part 58, OECD
- Responsibilities: Management, Study director, QA, analysts
- Special organizational requirements
- GLP studies: preparation, conduct, documentation
- SOP requirements: type, formats and enforcement
- Data generation and evaluation: raw data, intermediate results, final results
- Key requirements for equipment, facilities reference material, people
- Records keeping: format, length of time, archiving and reprocessing
Good Laboratory Practice Regulations - Introduction and Strategies for Implementation 2016 is intended for attendees from:
- QA managers and personnel
- Lab Supervisors and Managers
- GLP study directors
- GLP auditors
- Consultants
- Analysts
