VCU Human Research Protection Program (HRPP) Blog

The VCU HRPP is dedicated to facilitating ethically and scientifically sound research through robust review of research projects and through effective education and outreach to the VCU research community.

Reminder: IRB Training on Regulatory Documentation – April 2022

Ethical and effective conduct of human research requires careful documentation and record retention. Sign up for a special training session to learn all about regulatory requirements and best practices for regulatory documentation in human research! Sessions will be held virtually using Zoom, on the following dates: Wednesday, April 13, 9am-10am ET (Register here) Friday, April […]

RAMS-IRB will be patched 3/16/2022 6pm

As a reminder, the RAMS-IRB system will be patched tomorrow night (3/16/2022) from approximately 6pm – 11pm ET. Be sure to save your work before the system goes down. For a description of what updates are included in this patch, please refer to the summary of the changes below: Please contact the assigned IRB coordinator for […]

Education & Outreach Perspectives: Reportable Events

The VCU HRPP’s Education & Outreach Team is composed of professionals who are experts in the field of human research regulations. The unit delivers education and training to IRB members, to ensure high-quality and efficient reviews of research by IRB members. In addition, the unit also engages in education and outreach efforts to the VCU […]

PAMQuIP Perspectives: Reportable Events

The VCU HRPP’s Post-Approval  Monitoring and Quality Improvement (PAMQuIP) Team is tasked with providing ongoing oversight and monitoring of human research, following initial approval by the IRB. They help study teams ensure that their research is operationalized in compliance with regulation and in compliance with the IRB-approved protocol. The team is composed of Elizabeth Marlowe, […]

IRB Reliance Perspectives: Reportable Events

The VCU HRPP’s IRB Reliance Team is tasked with managing studies that engage in reliance agreements that cede IRB review to another, non-VCU IRB, or which allow the VCU IRB to review for multiple, non-VCU research sites. They manage externally reviewed research, such as research reviewed by WCG, Advarra, or another institution’s IRB. They also […]

IRB Analyst Perspectives: Reportable Events

The VCU HRPP’s IRB Analysts are professionals who are tasked with reviewing and approving minimal risk research at VCU. They independently review and approve expedited research protocols, perform exempt determinations, and make determinations of “Not Human Subjects Research.” As part of their work, they engage closely with investigators to provide expert regulatory guidance, including pre-submission […]

IRB Administrator Perspectives: Reportable Events

The VCU HRPP’s IRB Administrators are professionals who are tasked with ensuring submissions to the convened panel are ready for review at meetings, managing IRB meetings and providing expert regulatory advice, and working closely with investigators to help them respond to requests for changes or information from the convened panel. In this article, the IRB […]

IRB Chair Perspectives: Reportable Events

Dr. Ron Evans is an Associate Professor in the Department of Kinesiology and Health Sciences and currently serves as Chair of the VCU IRB Social Behavioral/Biomedical panel.  Dr. Evans has been a faculty member at VCU since 2003 and an IRB member since 2005.  Prior to his current role on the Social Behavioral/Biomedical panel, Dr. […]

IRB Director Perspectives: Reportable Events

Reportable Events: What should be reported to the IRB? By: Sanjur Brooks, DPS, MA The institutional review board (IRB) is an independent board federally mandated to review and monitor research involving intervention and/or interactions with human participants while ensuring the protection of their rights and welfare as research participants. Researchers, regardless of risk level, must […]

New IRB Training on Regulatory Documentation – April 2022

Ethical and effective conduct of human research requires careful documentation and record retention. Sign up for a special training session to learn all about regulatory requirements and best practices for regulatory documentation in human research! Sessions will be held virtually using Zoom, on the following dates: Wednesday, April 13, 9am-10am ET (Register here) Friday, April […]

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