IRB-Ready Study Builder
Configure participant flows, informed consent, data collection instruments, and eligibility criteria with our no-code study builder — designed to meet IRB requirements from day one.
Researchers & Universities
Translara gives research teams the infrastructure to design, deploy, and evaluate digital health interventions — without building a development team or compromising research rigor.
Configure participant flows, informed consent, data collection instruments, and eligibility criteria with our no-code study builder — designed to meet IRB requirements from day one.
Automate literature synthesis, clinical note analysis, and data extraction using Anthropic Claude and other foundational AI — freeing your team for higher-value research work.
Real-time dashboards showing participant enrollment, engagement, and outcome data — formatted for NIH progress reports, foundation grant requirements, and institutional reporting.
Multilingual AI support, mobile-first design, and culturally adapted content allow you to recruit and retain research participants from underrepresented communities.
HIPAA, 21 CFR Part 11, and IRB protocol support — with complete audit trails, data export capabilities, and documented security controls for research integrity.
Deploy web portals, mobile apps, and AI chat assistants that engage research participants in real-world settings — collecting longitudinal data beyond the clinical visit.
"The biggest barrier to translational research is not the idea — it's the gap between a validated protocol and a working digital system that can reach real patients at scale."
Connect with our team to explore how Intellicare can support your caregiver programs, nursing science research, or clinical support initiatives.