Session Information
2009 BIO International Convention
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Regulatory Best Practices for Emerging Companies & First-Time Filers
Track : Achieving Regulatory Approval
Program Code: 3009
Date: Tuesday, May 19, 2009
Time: 8:00 AM to 9:30 AM  EST
Location: B315
SPEAKER (S):
Wilson Bryan, MD, Biologics Consulting Group
Pamela Douglas, MBA, Booz Allen Hamilton
Ulrich Grau, Lux Biosciences, Inc
Christopher Joneckis, PhD, Senior Advisor For Chemistry Manufacturing and Control Issues, U.S. Food and Drug Administration
David Morse, PhD, PAREXEL Consulting
Description
Companies fi ling their fi rst NDA or BLA have a significantly lower likelihood of receiving first-cycle approval. Some factors contributing to this fact were discussed in an independent evaluation of FDA's first-cycle review performance, conducted by Booz Allen. This session, which specifically targets emerging and first-time filer companies, will further explore these factors from the perspective of different industry stakeholders,including representatives from industry and regulatory authorities. Panelists will also discuss best practices and offer recommendations to emerging companies on how to prepare for and execute against their first product approval application.

• Share relevant perspectives from Booz Allen's First-Cycle Evaluation and additional studies
• Highlight issues facing emerging companies and first-time filers
• Provide tools and best practices


Audio Synchronized to PowerPoint
(Code: 3009)
  
This session is a part of: