OHRP

Just another OMRF Labs site

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  • Agenda / Educational Materials

Agenda / Educational Materials

TIME DURATION SESSION
8:00 – 8:30 30 min Registration and Breakfast
8:30 – 8:40 10 min Welcome and Introductions (Organizers & OHRP)
8:40 – 9:55 75 min Overview of the Regulations and How to Apply Them (slides below)
Misti Ault Anderson, OHRP
9:55 – 10:50 55  minutes Evidence Based Practice (EBP) and Research Under the Common Rule**

Stacie Merritt, St. John’s Hospital

Jaime O. Hernandez, OHRP

10:50 – 11:00 10 min Break
11:00 – 12:00 60 minutes The Subject Perspective: A Panel Discussion**

Stacie Merritt, St. John’s Hospital

12:00 – 13:00 60 min Networking lunch
13:00 – 14:00 60 min Secondary Research with Data, Biospecimens, and Private Information (slides below)
Jaime O. Hernandez, OHRP
14:00 – 14:10 10 min Break
14:10 – 15:00 60 min Critical Review of a Clinical Research Protocol**

Yvonne Lau, OHRP

Misti Ault Anderson, OHRP

15:00 – 16:15 65 min Informed Consent: Putting it into Practice**

Yvonne Lau, OHRP

16:15 – 16:30 15 min Closing Remarks & Final Questions

Downloadable Agenda

Overview of Regulations and How to Apply Them

Evidence Based Practice (EBP) and Research under the Common Rule

Secondary Research with Data, Biospecimens, and Private Information

Food and beverages provided courtesy of Complion, St. John Medical Center, and the Oklahoma Medical Research Foundation. OHRP funding does not support this portion of the event.

Workshop sessions that are marked with a double asterisk (**) on the agenda meet the criteria in the Certified IRB Professional (CIP) recertification guidelines at www.primr.org/Subpage.aspx?id=1579. These sessions are eligible as accredited continuing education units for CIP and SoCRA accreditation. A maximum of 4.0 hours of CIP or SoCRA continuing education credits can be claimed.

PDF slides will be available for download prior to the workshop.

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