Training for the Community: Single IRB and Multi-Site Research
This is a recording of the HRPP Toolkit Training for the Community: Single IRB and Multi-Site Research presented on Friday, June 30, 2023 from 12:00-1:00pm via Zoom.
HRPP Toolkit Go-Live
The VCU Human Research Protection Program (HRPP) is pleased to announce that as the next milestone of the HRPP Transformation Project, the HRPP Toolkit will go live on the VCU HRPP website on July 14, 2023. The HRPP toolkit is a comprehensive set of workflows, standard operating procedures, checklists, worksheets, and templates. It is implemented […]
Training For the Community: Vulnerable Populations
This is a recording of the HRPP Toolkit Training for the Community: Vulnerable Populations presented on Friday, June 16, 2023 from 12:00-1:00pm via Zoom.
HRPP Newsletter Volume 008 | June 2023
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Researchers Separating From VCU Must Close or Amend Studies Prior to Separation
IRB Requirements for Separating PIs A Principal Investigator (PI) who is leaving the institution and who no longer meets the PI eligibility requirements may not continue to serve as Principal Investigator on research conducted under the VCU IRB approval. When a PI is planning to separate from VCU, they must address any studies they have […]
Training For the Community: Informed Consent
This is a copy of the presentation slides used for the HRPP Toolkit Training for the Community: Informed Consent presented on Friday, June 2, 2023 from 12:00-1:00pm via Zoom.
REMINDER: New Tools to Assist with IRB Submissions
PLEASE NOTE: Updated links to Protocol Templates provided 8/30/2023 Protocol templates are required for use effective today, June 1, 2023. New IRB submissions that do not contain a protocol will be returned to the researcher after today. If the IRB submission does not have a protocol provided by the sponsor, the use of HRP-503 or […]
HRPP Newsletter Volume 007 | May 2023
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Training For the Community: Clinical Drug and Device Trial Considerations
This is a recording of the HRPP Toolkit Training for the Community: Clinical Drug and Device Trial Considerations presented on Friday, May 19, 2023 from 12:00-1:00pm via Zoom. The links referenced in this presentation are: HRPP Toolkit Protocol Templates – required as of June 1, 2023 Future Training for the Community Sessions – please register […]
RAMS-IRB Updates with Protocol Launch
Protocol templates are required for use effective June 1, 2023. New IRB submissions that do not contain aprotocol will be returned to the researcher after this date. RAMS-IRB updates to reduce duplication between the submission smartform and protocol will be live June 1, 2023. The system will be more comprehensively updated later this fall – […]