| DATE |
TOPIC (Zoom Link/Recording) |
PRESENTATION |
| 10/05/2022 |
Overview of the IRB |
PPT / PDF |
| 11/09/2022 |
Database & Repository Research |
PPT / PDF |
| 12/07/2022 |
Reportable New Information
|
PPT / PDF |
| 01/11/2023 |
Emergency Preparedness in Research |
PPT / PDF |
| 02/01/2023 |
Informed Consents & HIPAA Authorizations (no recording)
|
PPT / PDF |
| 03/01/2023 |
Renewals |
PPT / PDF |
| 04/05/2023 |
Regulatory Binders |
PPT / PDF |
| 05/03/2023 |
Expanded Access Use of Test Article |
PPT / PDF |
| 06/07/2023 |
Non-Human Subjects Research Determinations |
PPT / PDF |
| 07/05/2023 |
Reliance |
PPT / PDF |
| 08/02/2023 |
Study Team Regulatory Responsibilities |
PPT / PDF
|
| 09/06/2023 |
FDA's IRB Inspection: A Post-Mortem |
PPT / PDF |
| 10/04/2023 |
Exempt Determinations & Limited IRB Review |
PPT / PDF |
| 11/01/2023 |
Expedited Review |
PPT / PDF |
| 12/06/2023 |
Full Board Review |
PPT / PDF |
| 01/10/2024 |
Informed Consent |
PPT / PDF |
| 02/07/2024 |
Amendments |
PPT / PDF |
| 03/06/2024 |
Closing a Study (Cancelled) |
PPT / PDF |
| 04/03/2024 |
Overview of the Office of Research Services |
PPT / PDF |
