Session Information
2008 BIO International Convention
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Developing Efficient Operations to Enable Collaborative Clinical Development
Track : Clinical Research/Clinical Trials
Program Code: 1472
Date: Thursday, June 19, 2008
Time: 8:30 AM to 10:00 AM  EST
Location: 32AB
CHAIR (S):
Mark Mynhier, MBA, Director , Pittiglio Rabin Todd & Mcgrath
David Nellesen, PhD, MBA, Life Sciences Industry Consultant , Pittiglio Rabin Todd & Mcgrath
SPEAKER (S):
Kim Davis, JD, AssocJDiate General Counsel , Amgen
Renee Gade, Global Director of CRO Operations , Covance, Inc
Sophie Visonneau, PhD, Director, Clinical Operations , Biogen Idec, Inc
Description
"Biopharmaceutical companies continue to face operational roadblocks in completing clinical trials on time and on budget. These roadblocks can stem from a variety of sources, including inadequate planning, poor execution and inconsistent expectations. This panel of biopharma and CRO experts will reveal proven methods for overcoming these obstacles and provide insights on how to build successful long-term relationships between biopharm and CROs companies."

Objective1: Discuss successful methods for establishing and maintaining effective collaborations from three perspectives: CRO, legal and clinical development.

Objective2: Identify efficient contract management processes.

Objective3: Discuss best practices for the governance of collaborative relationships.




Streaming Audio with
PowerPoint Slides
(Code: 1472)
  
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