MediTrials
Clinical research and N-of-1 trial management suite for precision medicine and evidence-based care in LMIC settings.
End-to-end clinical trial management from study design to analysis and publication.
Design and manage N-of-1 clinical trials with crossover protocols, randomisation, and blinding support.
Protocol builder with templates for RCTs, observational studies, and quality improvement research.
Recruitment, enrollment, consent management, and participant tracking through trial lifecycle.
Electronic data capture with configurable case report forms, validation rules, and offline support.
Statistical analysis tools with visualisation, Bayesian methods, and automated reporting.
Institutional Review Board submission tracking, ethics approvals, and amendment management.