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List of key usage scenarios supported by BRIDG
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- Submission of study data to a central repository
- Clinical trial participant registration, and submission of the registration data to ClinicalTrials.gov and other international registries
- Submitting data to research repositories, such as oncology data for the SEER Registry
- Submit subject lab data to CRO and/or sponsor (similar to TCB Use case 3)
- Study setup, management, and site network management
- Sharing protocol and CRF metadata and subject data among trial stakeholders
- Adverse Event reporting