List of key usage scenarios supported by BRIDG

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

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