Validation of Analytical Procedures for Use in the Pharmaceutical Industry 2012 is a webinar that covers topics such as:
- ICH and USP guidelines for procedure validation
- Review of procedures used in assessing quality, safety and efficacy of drug products
- Good Laboratory Practice (GLP)
- ICH guidelines and Good Manufacturing Practice (GMP)
- Key aspects involved in procedure validation
- Phases of clinical trials and the path to commercialization
- Laboratory responsibility to assuring validation is robust
- Complex procedures
Validation of Analytical Procedures for Use in the Pharmaceutical Industry 2012 brings together QC validation or technical transfer groups, All QC functions, Contract laboratory testing facilities, Commercial testing facilities and Project support functions.
