Validation of Analytical Procedures for Use in the Pharmaceutical Industry 2012

24 Feb 2012

Webinar

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.

Past Events

Validation of Analytical Procedures for Use in the Pharmaceutical Industry 2012 - 24 Feb 2012, Webinar (24698)

Validation of Analytical Procedures for Use in the Pharmaceutical Industry 2026

Important

Please, check "Validation of Analytical Procedures for Use in the Pharmaceutical Industry" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance

Health & Medicine: Medical laboratories, Pharma

Science: Laboratories

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