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Advisory Panel on Research

October 24, 2007
Renaissance M Street Hotel

Agenda

8:30 a.m. - Introductions and Welcome

Larry J. Shapiro, M.D. - APR Chair
David Korn, M.D. - AAMC Sr. Vice President, Division of Biomedical and Health Sciences Research

8:35 a.m. - NIH Appropriations and Legislative Report

David Moore - AAMC Sr. Associate Vice President, Office of Government Relations

9 a.m. - Clinical Trials Registration

Deborah A. Zarin, M.D. - NIH National Library of Medicine

Discussion with Panel
Dr. Larry Shapiro

The panel will review the progress of the NIH clinical trials registry and the issues that have emerged to date in light of the APR's earlier examination of this issue in 2005. The panel will also consider the pros and cons of new legislation on clinical trials databases, and AAMC position.

10 a.m. - Input for NIH Research Support Systems Initiatives

Howard B. Dickler, M.D. - AAMC Director, Clinical Research

Dr. Dickler will review the NIH request for input and activities looking at reform of peer review systems and other issues, and will present the AAMC's several recommendations for further discussion by the panel.

10:45 a.m. - Update on the Clinical and Translational Science Awards Program

Barbara Alving, M.D. - Director, NIH National Center for Research Resources
Anthony Hayward, M.D., Ph.D. - Associate Director, Division for Clinical Research Resources

Dr. Hayward has been invited to present on the status of the CTSA program in the context of NIH and NCRR budgets. Dr. Alving will join in discussion with the panel.

12:00 p.m. - Working Lunch

Dr. Larry Shapiro, Dr. David Korn, and AAMC Staff

The panel will wrap up morning discussions and discuss planning for future initiatives that largely follow-on from earlier APR meetings, including support of "T2" research (and population health, health services, etc.) from October 2006 and options for universities to restructure research programs in light of probable static or contracting purchasing power of future NIH budgets.

  1. Use of patient population datasets to support health research
  2. Workshop on good practices in university collaborations (identifying scale economies, minimizing redundancy, etc.)
  3. "Trusted Intermediaries" for data in genomic research

2:30 p.m. - Adjourn


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