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SACGHS February 4-5, 2010 - Presentation Materials
Twenty First Meeting
Washington, DC
  Breakout Webcasts  
   Morning Session (before break)
 
   Morning Session (after break)
 
   Afternoon Session (before break)
 
   Morning Session (after break)
 
   Day 2 Webcasts
 
  Presentation Materials for Day 1  
   Update on the Clinical Utility and Comparative Effectiveness Task Force
Marc Williams, M.D.
SACGHS Member
 
   Briefing on the Secretary's Advisory Committee on Heritable Disorders in Newborns and Children (ACHDNC) Education Subcommittee
Jana Monaco
Co-Chair, Education and Training Subcommittee, ACHDNC
 
   Overview of Draft Report and Draft Recommendations
Barbara Burns McGrath, R.N., Ph.D.
SACGHS Member
 
   Future Directions in Health Information Technology
Joyce Mitchell, Ph.D.
Professor and Chair, Department of Biomedical Informatics
University of Utah School of Medicine
 
   Introduction to Genomic Data Sharing
Charmaine Royal, Ph.D.
SACGHS Member
 
   Review of Federal Activities Related to Genomic Data Sharing
Laura Lyman Rodriguez, Ph.D.
Acting Director, Office of Policy, Communications, and Education
National Human Genome Research Institute
 
   Genomic Data Sharing: Health Care Systems Model
Catherine Schaefer, Ph.D.
Executive Director, Research Program
Kaiser Permanente
 
   Genomic Data Sharing: Academic Model
Daniel Masys, M.D.
Professor and Chair, Biomedical Informatics
Vanderbilt University
 
   Genomic Data Sharing: Government Model
Laura Lyman Rodriguez, Ph.D.
Acting Director, Office of Policy, Communications, and Education
National Human Genome Research Institute
 
   Genomic Data Sharing: Commercial Model
Mark Hoffman, Ph.D.
Director, Translational Medicine
Cerner Corporation
 
   Genomic Data Sharing: Consumer-Controlled Model
Robert H. Shelton, M.B.A.
Co-Founder, Chairman, Chief Executive Officer
Private Access, Inc.
 
  Presentation Materials for Day 2  
   Carrier Screening for Sickle Cell Disease
R. Rodney Howell, M.D.
Chair
Advisory Committee on Heritable Disorders in Newborns and Children
 
   Development of an FDA Adverse Event Reporting Mechanism for Laboratory Developed Tests
Alberto Gutierrez, Ph.D.
Office of In Vitro Diagnostic Device Evaluation and Safety
Food and Drug Administration
 
   ONC and HITECH
David R. Hunt, MD, FACS
Medical Officer
Office of the National Coordinator for Health IT
 
   MEDCAC Meeting on Pharmacogenomic Testing for Anticancer Therapie
Jeffrey Roche, M.D., M.P.H.
Coverage & Analysis Group, Office of Clinical Standards and Quality
Centers for Medicare & Medicaid Services
 
   AHRQ Evidence-Based Reports Relevant to Genetic Testing
Gurvaneet Randhawa, M.D., M.P.H.
Center for Outcomes and Evidence
Agency for Healthcare Research and Quality
 
   Development of Genomics Objectives for Healthy People 2020
Muin Khoury, M.D., Ph.D.
National Office of Public Health Genomics
Centers for Disease Control and Prevention
 
   Committee Report on the Retention and Use of Residual Dried Blood Spot Specimens after Newborn Screening
R. Rodney Howell, M.D.
Chair
Advisory Committee on Heritable Disorders in Newborns and Children
 
 
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