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 |
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.