Time:December 03-03, 2013
Organizer:European Pharmaceutical Review
Microbial excursions as a result of an out of specification result from a quality control test can be time consuming and costly. The investigation of the root cause, analysis of the risk to the product, and determination of corrective/preventative actions take hours of manpower and resources and often are caused by issues around personnel practices, keying errors, and incubation errors.
During this webinar learn from industry experts some practices to help better manage the investigation process and how to design processes to minimize unnecessary excursions.
Attendees will learn:
" What is an excursion?
" How to identify risk in an excursion
" Tools to help manage the process
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