This 3-hr virtual session will cover pharmaceutical stability study requirements for Phase I, Phase II, Phase III clinical studies, show how to choose the right stability methods and specifications and review common pitfalls in pharmaceutical stability programs.
Why Should You Attend:
The Stability Program is a key component of Product Development. The time scale for a stability studies is relative long, ranging from 2-3 years and is very often on the Critical Path of the Product Development Project. Errors found in the study design, can result in major delays in the project filing. A well designed Stability protocol can result in significant savings during Product Development and after product approval.
For Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702014?channel=eventsbot