Validation of Analytical Procedures for Use in the Pharmaceutical Industry 2012
February 24, 2012(Ended)
Online Webinar
Validation of Analytical Procedures for Use in the Pharmaceutical Industry 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 brings together QC validation or technical transfer groups, All QC functions, Contract laboratory testing facilities, Commercial testing facilities and Project support functions.
Prices *
699-2499 US Dollar
Exhibition
No exhibition
Organization
Categories
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
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