Portal, billing and business requirements · C0824
Does AuroraMed support research consent (eConsent), IRB documents, participant recruitment, CTMS integration, biospecimen tracking and clinical-trial billing separation?
Designed, not yet built
Short answer
Designed, not built: there is no code for this in the pilot. REQ-2451 says the system must support research consent (eConsent), IRB documents, participant recruitment, CTMS integration, biospecimen tracking and clinical-trial billing separation. Its acceptance check: participant flagged; billing routes by rule.
This is designed, not built.
- Specification item
- REQ-2451
- Specification priority
- P2 (of P0 to P3)
- Tiers
- Medium, Large
Status as of September 30, 2026. Version 0.2.0, synthetic data only. See what's built today. Not legal, medical or security advice.
Related answers
See it in context: Research and clinical trials · Search the help center · Ask a question