Portal, billing and business requirements
Research and clinical trials
IRB, consent, trials.
How to read status labels: In the pilot (v0.2.0, synthetic data) Simulated in the pilot Coming (Wave 2, rolling out) Designed, not yet built Open decision Not offered / no claim made Planned partner integration
C0824Does AuroraMed support research consent (eConsent), IRB documents, participant recruitment, CTMS integration, biospecimen tracking and clinical-trial billing separation?
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.
C0825Does AuroraMed support research datasets (limited/de-identified/OMOP) under DUA?
REQ-2452 is a medium-priority requirement for the medium and large tiers: the system must support research datasets (limited/de-identified/OMOP) under DUA. This is on the design side of the line. Nothing in v0.2.0 does it. To verify it, the specification says extract logs approvals.