University of Southern California , Irvine, CA, USA
Jan 9 2011 8:00AM - Jan 12 2011 5:15PM
Learn how to apply regulatory concepts to ensure compliant IND submissions to the FDA. Gain insight into the regulatory background of the NDA, preparing an NDA, and postapproval activities. The course focuses on drug and well characterized biological products and not the regulatory process for devices, generic products, or traditional biologics. Event Code:
11413
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Registration:
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Contact Information: For detailed program information including faculty and topics, please contact: Susan Mazak Tel. +1-215-442-6183 Email Susan.Mazak@diahome.org
If you have not received confirmation within 5 business days, please contact: DIA Tel. +1-215-442-6100 Fax +1-215-442-6199 Email confirmationservices@diahome.org
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