We conduct monthly seminar sessions to inform faculty, students and staff about the federal regulations and institutional policies that impact researchers at MU.
Upcoming HRPP/IRB Seminars
Seminars are held on the second Monday of the month from 2-3 p.m. on Zoom. (Request Zoom link)
- August (pre-recorded Office for Human Research Protections training) – Participant-Centered Informed Consent Training This seminar is for anyone in the research community who plans, writes or reviews consent forms for research involving human participants. It will cover a participant-centered approach to creating consent forms. It includes examples and interactive exercises.
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 | |
---|---|---|
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
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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 | ![]() |
2023-04 | External sponsors: IRB requirements 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
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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 | ![]() |