From protocol design to analysis-ready data, eRIC AI applies Artificial
Intelligence deliberately to remove operational bottlenecks in clinical
trials — with humans firmly in control.
From protocol design to analysis-ready data, eRIC AI applies Artificial
Intelligence deliberately to remove operational bottlenecks in clinical
trials — with humans firmly in control.
From protocol design to analysis-ready data, eRIC AI applies Artificial
Intelligence deliberately to remove operational bottlenecks in clinical
trials — with humans firmly in control.
Our platform is built so your team does not need a six-week implementation project to use it. A single 90-minute guided onboarding session is enough for most teams to start managing live study data the same day — no heavy customisation, no steep learning curve.
Every engagement includes hands-on support from GCP-trained clinical research professionals — not a ticket queue. They train your team, sit in on study set-up, and stay reachable through database lock.
Our platform is built so your team does not need a six-week implementation project to use it. A single 90-minute guided onboarding session is enough for most teams to start managing live study data the same day — no heavy customisation, no steep learning curve.
Every engagement includes hands-on support from GCP-trained clinical research professionals — not a ticket queue. They train your team, sit in on study set-up, and stay reachable through database lock.
Our platform is built so your team does not need a six-week implementation project to use it. A single 90-minute guided onboarding session is enough for most teams to start managing live study data the same day — no heavy customisation, no steep learning curve.
Every engagement includes hands-on support from GCP-trained clinical research professionals — not a ticket queue. They train your team, sit in on study set-up, and stay reachable through database lock.
Trials
Patients
Repeat Business
Recruitment
Countries
Trials
Patients
Repeat Business
Recruitment
Countries
Trials
Patients
Repeat Business
Recruitment
Countries
Rapid protocol-to-CRF design with edit checks and SDTM-ready structures.
AI-assisted ingestion of scanned source documents with PHI de-identification.
Remote, risk-based monitoring using de-identified source data.
Real-time analytics and analysis-ready datasets.
AI-assisted drafting of clinical documents with human review.
Continuous eTMF completeness and inspection readiness.
Predictive insights into timelines, risks, and execution.
Choose the plan that fits your workflow
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Responsible AI for Regulated Clinical Environments
19 days — database design complete (USA, 4 sites, 60 subjects).
Within 5 weeks of signing — first site initiated.
27% faster than the industry average.
eRIC AI is built to deliver it.