OCTA Contracting Documents
| A chart and step by step guide to the OCTA contracting process | |
| Required for all agreements related to clinical trials. | |
| Required prior to the execution of any clinical trial contracts or grants. | |
| Required to collect mandatory information regarding financial conflict of interest. | |
| Submitted at the time of IRB submission application for new protocols, and again at continuing review. | |
| Detailed instructions for completing a Human Research Billing Analysis Form. |