This is just a snapshot of Day Two.
For full details please download our brochure.
| 8:45 |
Morning Coffee and Chairperson's Day One Recap Co-Chair: Whaijen Soo, MD, PhD Senior Vice President of Medical Research
|
| 9:00 |
Creating a Standardized Approach and Tackling the Challenges of Microdosing Stephen R. Dueker, PhD CEO VITALEA SCIENCE |
| 9:45 |
KEYNOTE SPEAKER Hamilton Jordan Bestselling Author of "No Such Thing As a Bad Day", |
| 10:45 | Networking Break |
| 11:15 |
Part I-Process, Approach and Standards - Learning from the TeGenero & Parexel TGN1412 London Phase I Study Part II - Overseas Phase I Trials: Examining the Status and Future of Partnerships Abroad Francis P. Crawley Director General
|
| 12:15-2:00 | Luncheon |
| 2:00 |
Dealing with IRBs to Promote Timely, Efficient and Compliant Review Lynn A. Meyer President CIP, CIM,
|
| 2:30 |
How Exploratory INDs Can Help You Use Less Resources John Wagner, MD Executive Director, Clinical Pharmacology |
| 3:00 |
Steady Enrollment and Optimal Trial Metrics Can Become Reality: The Use of Key Enrollment Optimization Processes, Clinical Investigative Networks and eClinical Processes to Facilitate Cost Effective Clinical Trials Michael Pozsgai Global Optimization Consultant
Lee Scheible, RPh Senior Medical Consultant
|
| 4:00 | Personalized Medicine- Change in the Industry and it's Effect on the Future of Phase I Trials |
| 4:30 | Close of Program |
Copyright 2003-2006 IIR Holdings, Ltd. All rights Reserved