Appendix D

Meeting Agendas

Thursday, February 3, 2011

Keck Center of the National Academies
500 Fifth Street, NW
Washington, DC 20001

1:00-1:15 pm

Committee Introductions and Chair’s Opening Jane Henney Committee Chair

   
1:10-1:30 pm

Charge to the Committee
Lawrence Deyton, M.D., M.S.P.H. Director Center for Tobacco Products U.S. Food and Drug Administration (FDA)

   
1:30-2:00 pm

Discussion About the Charge
Committee and FDA Representatives

   
2:00-3:00 pm

Public Comment

   
3:00 pm

Adjourn



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OCR for page 347
Appendix D Meeting Agendas Thursday, February 3, 2011 Keck Center of the National Academies 500 Fifth Street, NW Washington, DC 20001 1:00–1:15 pm Committee Introductions and Chair’s Opening Statement Jane Henney Committee Chair 1:10–1:30 pm Charge to the Committee Lawrence Deyton, M.D., M.S.P.H. Director Center for Tobacco Products U.S. Food and Drug Administration (FDA) 1:30–2:00 pm Discussion About the Charge Committee and FDA Representatives 2:00–3:00 pm Public Comment 3:00 pm Adjourn 347

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348 STUDIES ON MODIFIED RISK TOBACCO PRODUCTS Monday, May 9, 2011 Embassy Suites 900 Tenth Street, NW Washington, DC 20001 9:45–10:00 am Welcome and Introductions Jane Henney Committee Chair 10:00–11:30 am Panel Discussion I: Tobacco Manufacturers Moderator: Peter Honig 10:00–11:00 am: Presentations by industry representatives 11:00–11:30 am: Questions from the Committee • Introduction Standards for pre-clinical studies Mike Ogden Senior Director of Regulatory Oversight R.J. Reynolds Tobacco Company • Standards for studies on in vitro models of disease Chris Proctor Chief Scientific Officer British American Tobacco • Standards for clinical studies and biomarkers Mohamadi Sarkar Senior Principal Research Scientist Altria Client Services • Population communication and risk perception Lars Erik Rutqvist Senior Vice President for Scientific Affairs Swedish Match • Summary J. Daniel Heck Principal Scientist Lorillard Tobacco Company

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349 APPENDIX D 11:30 am– Andrew Salmon 12:00 pm Senior Toxicologist and Chief Air Toxicology and Risk Assessment Section Office of Environmental Health Hazard Assessment California Environmental Protection Agency 12:00–1:00 pm Lunch 1:00–1:30 pm David Jacobson-Kram Associate Director of Pharmacology and Toxicology Office of New Drugs Food and Drug Administration 1:30–2:00 pm Peter G. Shields Professor of Medicine and Oncology Deputy Director, Lombardi Comprehensive Cancer Center Georgetown University Mirjana Djordjevic Health Scientist Administrator Tobacco Control Research Branch National Cancer Institute 2:00–2:30 pm John Baron Professor of Medicine Dartmouth Medical School 2:30–2:45 pm Break 2:45–3:15 pm Brenda Edwards Associate Director Surveillance Research Program National Cancer Institute 3:15–3:45 pm Ruth S. Day Director Medical Cognition Laboratory Duke University 3:45–4:15 pm David Mendez Associate Professor Department of Health Management and Policy University of Michigan School of Public Health

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350 STUDIES ON MODIFIED RISK TOBACCO PRODUCTS 4:15–4:30 pm Break 4:30–6:00 pm Panel Discussion II: public health representatives Moderator: Dan Carpenter 4:30–5:30 pm: Presentations by public health representatives 5:30–6:00 pm: Questions from the Committee • David Abrams Executive Director The Schroeder Institute for Tobacco Research and Policy Studies Professor, Department of Health, Behavior and Society The Johns Hopkins Bloomberg School of Public Health • Tom Glynn Director, Cancer Science and Trends Director, International Cancer Control American Cancer Society • Mark Greenwold Director, Regulatory Affairs Campaign for Tobacco-Free Kids • Rose Marie Robertson Chief Science Officer American Heart Association • Mitch Zeller Vice President for Policy and Strategic Communications Pinney Associates 6:00 pm Adjourn