List of key usage scenarios supported by BRIDG

From HL7Wiki
Jump to: navigation, search
  1. Submission of study data to a central repository
  2. Clinical trial participant registration, and submission of the registration data to 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

Copyright © Health Level Seven International ® ALL RIGHTS RESERVED. The reproduction of this material in any form is strictly forbidden without the written permission of the publisher.