OHRP Exploratory Workshop Tentative Agenda

Meeting New Challenges in Informed Consent in Clinical Research

Friday, September 7, 2018
8:00a.m. - 5:00p.m.

Livestream Webcast

Session A: Laying the groundwork for meaningful informed consent

David Strauss, MD; Austen Riggs Center
Danielle Bromwich, PhD; University of Massachusetts Boston
Joseph Millum, PhD; NIH Clinical Center Department of Bioethics
Rebecca Dresser, JD; Washington University in St. Louis
Baruch Fischhoff, PhD; Carnegie Mellon University

Session B: Effectively presenting information to facilitate high-quality decision-making

Christine Grady, MSN, PhD; NIH Clinical Center Department of Bioethics
Angela Fagerlin, PhD; University of Utah
Lisa Schwartz, MD, MS; Dartmouth University
Steven Woloshin, MD, MS; Dartmouth University
John Wilbanks; Sage Bionetworks
Megan Doerr, MS, CGC; Sage Bionetworks

Session C: Pragmatic clinical trials (PCT) — challenges and innovations in getting informed consent

Gregory Simon, MD, MPH; Kaiser Permanente Washington Health Research Institute
Ryan Ferguson, DSc, MPH; U.S. Department of Veterans Affairs
Sarah Leatherman, MA, PhD; U.S. Department of Veterans Affairs
George Annas, JD, MPH; Boston University

Session D: Delivery room research and the challenges for informed consent

Sara F. Goldkind, M.D., M.A.; Goldkind Consulting, L.L.C.

Neil Finer, MD; Sharp Mary Birch Hospital for Women & Newborns
Mark Schreiner, MD; Children’s Hospital of Philadelphia
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