Online Event - Paolo Alto, CA, United States
This webinar on lyophilization technology will provide you the understanding required to develop an optimized, cGMP compliant formulation that is specifically designed for lyophilization.
The topics described in this session will cover all of the aspects of understanding the justification for freeze-drying, the thermal properties of the formulation (crystalline, amorphous, mixed), the analytical techniques employed to characterize these systems, and how all of this information is used to develop a stable, optimized, cGMP compliant product. At the end of the session, the attendee will be able to develop a well-defined process for taking an empirical approach to designing formulations and the lyophilization cycles used to dry them. By understanding and applying these principles, companies have a much greater chance of getting products approved by the regulatory agencies than those companies that employ the “trial and error” approach to formulation and lyophilization cycle design.
Instructor: J. Jeff Schwegman
(Photo courtesy of http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702305?channel=allconf)
Thursday, May 10, 2012
Contact: 2600 E. Bayshore Road
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