The VCU Human Research Protection Program would like to inform the VCU research community about the availability of a new educational resource on the topic of re-consenting children who reach the age of majority during a research study. This 15 minute video lecture covers relevant definitions, requirements for parental permission and assent, as well as […]
Stacy West, MS, CIP, IRB Reliance Agreement Specialist, presents on submitting reliance requests to the VCU HRPP. Prevent extended delays in the process with West’s explanation of the screening process. You can also access the video here. For questions, please contact Stacy West, at irbreliance@vcu.edu or 804-827-1446
Are you participating in multi-site research that requires external IRB review? Stacy West and John Horigan will be presenting on everything you need to know about external IRB submissions (reliance agreements) at the monthly meeting of the One VCU Clinical Research Teams, on Tuesday, February 11th. Please see below for information on how to join […]
Registration is now open for new IRB workshops. Go to http://training.vcu.edu/ to register; search under category “IRB” Criteria for IRB Approval: Writing Submissions the IRB Can Approve Thursday, March 26, 2015; 10:00 – 11:30 am; BioTech One, Room 3060 (Medical Campus) Monday, March 30, 2015; 10:00 – 11:30 am; University Student Commons, Metro Room (Monroe Park Campus) Upon completion […]
The IRB is holding an interactive course to demonstrate RAMS-IRB to investigators and research personnel. Attendees will learn to navigate the RAMS-IRB system and will create a new protocol in the test environment. To register go to training.vcu.edu; search “IRB” Monroe Park Campus RAMS-IRB 101 Courses Friday, February 20, 2015; 10:00-11:30 am; Technology Administration Building, […]
RAMS-IRB 101 Interactive Courses Tuesday, July 29; 2-3:30 pm; Tompkins-McCaw Library Classroom Friday, August 22; 2:30-4:00 pm; Tompkins-McCaw Library Classroom Friday, September 26; 2-3:30 pm; Tompkins-McCaw Library Classroom The IRB is holding interactive RAMS-IRB 101 courses in order to demonstrate RAMS-IRB to researchers and study personnel. Attendees will practice navigating the RAMS-IRB system and will create a […]
RAMS-IRB 101 Interactive Course Friday, May 23; 2-3:30pm; Tompkins-McCaw Library Classroom The IRB is holding an interactive RAMS-IRB 101 course in order to demonstrate RAMS-IRB to researchers and study personnel. Attendees will practice navigating the RAMS-IRB system and will create a new submission in the RAMS-IRB training environment. Participants will also be shown where to access additional RAMS-IRB […]
“Clinicaltrials.gov – ramped up: Registering, reporting and consent language” Melanie Wiggins, Director, Office of Sponsored Programs – Industry Support & Monika S. Markowitz, Ph.D.,Dir, Office of Research Integrity and Ethics
“Protecting Human Subjects in Biomedical Research: Working with the IRB” Benjamin Van Tassell, PharmD, BCPS, Assistant Professor & Research Professor & Monika Markowitz, Ph.D., Dir. Office of Integrity and Ethics
“Progress to the Needs Assessment Survey” Dr. Enid Virago, Research Liaison Specialist for Human Research Protection, Office of Research Integrity and Ethics.