AIIA Clinical Trials Dashboard - a real-time, cloud-based, GCP-compliant Clinical Trial Management System (CTMS) for Ayurveda research, with CDISC/FHIR-interoperable data, role-based KPIs, and integrated ethics, regulatory (CTRI / NDCT Rules 2019) and pharma covigilance tracking.
Source
- Smart India Hackathon 2026 (opens in a new tab)SIH 2026Collection launched: 21 Aug 2026
Source summary
AIIA proposes a cloud clinical-trial management dashboard covering protocols, ethics approval, CTRI registration, recruitment, visits, deviations, data queries and close-out. Pharmacovigilance should track adverse-event reporting and standard dictionaries, with role-specific access and immutable ALCOA+ audit records. The requested interoperability includes CDISC, FHIR R4, EDC, hospital systems and ABDM, with consent, data-resident hosting and submission exports. Named regulatory/security standards are source requirements, not verified compliance claims; rollout can begin with core study tracking.