| Term | Description |
| Pre-screening | A basic check to see if you may qualify before official enrollment. |
| IRB | Institutional Review Board, which reviews research to protect participant rights. |
| Informed Consent | The process of understanding a trial before voluntarily agreeing to join. |
| De-identified Data | Data that has been stripped of personal identifiers. |
| Sponsor | A company or organization funding the clinical trial. |
| Site | A hospital, clinic, or research facility running the trial. |
| CRO | Contract Research Organization that supports sponsor needs. |
| Dashboard | Your personalized control panel showing progress and activity. |
Leave a Reply