OVPRI Human Subject Research Protection Blog

The VCU Human Research Protection Program 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.

Category results for: IRB Education and Training

New Investigator Tips: What are the CITI Training Requirements at VCU?

Federal regulations for the protection of human subjects contain various areas of flexibility, where institutions are allowed to set policy and procedures for certain aspects of the conduct of human research. While many aspects of conducting human research remain the same between institutions, there are certain areas that can vary between institutions. This means investigators […]

FREE CEU: Free Workshop on Assent with Individuals with Communication Difficulties

The VCU HRPP Would like to notify the research community about a free workshop offering CEUs on the topic of assent with individuals with communication difficulties. The workshop is being held on Wednesday, June 29 at 3pm ET. Toward an Understanding of Assent with Individuals with Communication Difficulties. Presenter: Cody Morris, Ph.D., BCBA-D, LBA Seeking […]

New NIH Guidance on Informed Consent for Secondary Research with Data and Biospecimens

The VCU HRPP would like to draw the research community’s attention to a new resource made available by the NIH, on the topic of informed consent considerations for secondary research with data and specimens. This resource addresses only consent for the storage and sharing of data and biospecimens collected during a primary research protocol, for […]

IRB Chair Perspectives: The Importance of the Independence of IRBs

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. In this article, Dr. Evans reflects on the importance of the IRB […]

HRPP Director Perspectives: The Importance of the Independence of IRBs

Dr. Sanjur “Sandy” Brooks, DPS, MA, is the Director of the VCU Human Research Protection Program. In this article, she reflects on the importance of the IRB operating independently, free from undue influence or inducement. There is an inherent conflict and dichotomy in facilitating human subject research that is not always recognized by those of […]

Research Dean Perspectives: The Importance of the Independence of IRBs

Dr. Michael Donnenberg is the Senior Associate Dean for Research and Research Training and Professor of Internal Medicine and of Microbiology and Immunology in the VCU School of Medicine. In this article, he shares his thoughts on the topic of ethics and integrity, with an emphasis on the importance of the independent operation of the […]

Navigating RAMS-IRB to Save a Backup of the RAMS-IRB SmartForm/Protocol

This RAMS Gif Guide is intended for researchers and research teams using the RAMS-IRB system to manage IRB submissions. This guide will walk users through the process of saving a PDF version of the RAMS-IRB SmartForm/Protocol. Investigators and study teams are encouraged to regularly download a copy of the RAMS-IRB SmartForm/Protocol for each of their […]

Wright Center/IRB Virtual Consulting Hours – April 18 10am-1pm

Is your research project stuck? Come to consulting hours with the Wright Center and the VCU Human Research Protection Program! We’ll help you get unstuck. Consulting hours are being held virtually using Zoom on April 18th, from 10am-1pm ET. Consultants from various research areas are available to help you with study design, data questions, and […]

OHRP Virtual Webinar: A Conversation with IRB Professionals – April 27

Register now for OHRP’s 75 minute virtual webinar: A conversation with IRB professionals: Learn what they do and how they can help you navigate protecting human participants in research on Wednesday, April 27, 2022, at 3:00 PM EST. This webinar will cover the following: How IRBs support the preliminary reviews of research studies at institutions  What assistance IRBs can give […]

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 […]

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