'Human research protection programs' presentation slideshows

Human Research Protection Programs

1.19k views • 63 slides

Human Research Protection Programs

Human Research Protection Programs. Legal and Regulatory Issues Ann Sparkman UCSF Office of Legal Affairs February 18, 2008. GELSINGER CASE. Death of 18-year-old Jesse Gelsinger in study by University of Pennsylvania Institute for Gene Therapy

584 views • 45 slides

Institutional Review Boards (IRBs) and Human Subjects Research Protection Programs (HRPP) A SHORT COURSE

Institutional Review Boards (IRBs) and Human Subjects Research Protection Programs (HRPP) A SHORT COURSE. Course Content: Part 1: Brief Description of the IRB and Research at Tulane University Part 2: IRB Support Staff Functions Part 3: Researcher Responsibilities

900 views • 44 slides

Regulatory Challenges Lessons Learned from the OTC Gene Therapy Trial

Regulatory Challenges Lessons Learned from the OTC Gene Therapy Trial. James M. Wilson, M.D., Ph.D. Director, Gene Therapy Program Professor, Department of Pathology & Laboratory Medicine University of Pennsylvania 31 March 2011 2011 Institutional Review Board Annual Educational Conference.

699 views • 41 slides

IRB Presentation

Institutional Review of Research Involving Human Participants. IRB Presentation . University of Central Florida Office of Research & Commercialization 407-823-2901 or fax 407-823-3299 www.research.ucf.edu/Compliance/irb.html. University of Central Florida Institutional Review Board Overview.

802 views • 32 slides

HRPP METRICS

HRPP METRICS. Cynthia Monahan, MBA, CIP IRB Director Boston University Charles River Campus IRB. Table of Contents. Overview of Metrics IRB Metrics QI Program Metrics AAHRPP Metrics for Quality Improvement. What are Metrics?.

599 views • 24 slides

Human Research Protection Programs 1a: How to Navigate Human Subject Protection Regulations

Human Research Protection Programs 1a: How to Navigate Human Subject Protection Regulations . Sponsored by the American Society for Investigative Pathology Chair, Mark E. Sobel, M.D., Ph.D. Program. 3:00 p.m. Mark E. Sobel (ASIP) mesobel@asip.org Why all the fuss?

580 views • 23 slides

SACHRP Panel: Holding External IRBs Accountable

213 views • 11 slides

Keith Norris, M.D., Executive VP, Research and Health Affairs Charles Drew University

CTSA-NICHD Workshop on Comparing Institutional Review Board (IRB) Models for Multisite Pediatric Studies April 23, 2009. Keith Norris, M.D., Executive VP, Research and Health Affairs Charles Drew University. Our Reciprocal IRB Agreement. Cedars-Sinai Medical Center

211 views • 9 slides