Upcoming HRPP/IRB Seminars
We conduct monthly seminar sessions to inform faculty, students and staff about the federal regulations and institutional policies that impact researchers at MU. Seminars are held on the second Monday of the month from 2-3 p.m. on Zoom. (Request Zoom link)
- May 12th - Biospecimen Utilization in Human Subject Research: Regulatory Definitions, IRB Requirements, and Information for Investigators - Presented by Lori Wilcox, EdD, MS - Director HRPP/IRB
Do you have feedback or suggestions for the IRB? Submit feedback form here.
Previous HRPP/IRB Seminars
Below, you can access presentation PDFs from previous seminars using your MU login credentials and request the video presentation.
| Date | Title of seminar | Slide presentation image |
|---|---|---|
| 2025-02 | Legally effective informed consent PDF | Request video |  |
| 2024-12 | IRB determinations for not-human-subject activities PDF | Request video |  |
| 2024-11 | First steps with IRB PDF | Request video |  |
| 2024-10 | Q&A session PDF | Request video |  |
| 2024-09 | Investigator training, qualifications and responsibilities PDF | Request video |  |
| 2024-08 | Participant-centered informed consent Watch video |  |
| 2024-07 | Amendment form and process PDF | Request video |  |
| 2024-06 | CTSU: What can we do for you? PDF | Request video |  |
| 2024-05 | MU serving as the IRB of record for multisite studies PDF | Request video |  |
| 2024-04 | Privacy and confidentiality in research PDF | Request video |  |
| 2024-03 | MU research recruitment methods and advertisements PDF | Request video |  |
| 2024-02 | Reliance requests and collaborative exempt projects PDF | Request video | Image
|
| 2023-12 | Primary reasons IRB submissions are returned for correction PDF | Request video |  |
| 2023-11 | Engaged in human research PDF | Request video |  |
| 2023-10 | Event reporting and corrective action plans PDF | Request video |  |
| 2023-09 | How to prepare for an FDA inspection PDF | Request video |  |
| 2023-08 | OASH presentation: respecting persons PDF | View Recording |  |
| 2023-07 | Navigating the IRB exempt application PDF | Request video |  |
| 2023-06 | IRB application overview PDF | Request video |  |
| 2023-05 | IDS approval of IRB projects PDF | Request video |  |
| 2023-03 | Export controls, sanctions and research security PDF | Request video |  |
| 2023-02 | Interactions with sponsored programs PDF | Request video |  |
| 2023-01 | Web-based recruitment resources PDF | Request video |  |
| 2022-12 | IRB Review of supplements, food and cosmetics PDF | Request video |  |
| 2022-11 | Informed consent: ensuring comprehension and transparency PDF | Request video |  |
| 2022-10 | Student research project guidance PDF | Request video |  |
| 2022-07 | Working with industry: compliance PDF | Request video | Image
|
| 2022-06 | Noncompliance in human subjects research PDF | Request video |  |
| 2022 - 05 | IRB review of drugs/biologics and medical devices PDF | Request video |  |
| 2022 - 04 | Monitoring PDF | Request video |  |
| 2022 - 03 | Document changes in eCompliance PDF | Request video |  |
| 2022 - 01 | CITI program training PDF | Request video |  |
| 2021 - 12 | HRPP at MU: determining HSR criteria PDF | Request video |  |
| 2021 - 11 | HRPP at MU: recruitment of research participants PDF | Request video |  |
| 2021 - 05 | HRPP incidental findings in research PDF | Request video |  |