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.
eRIC AI agents work inside your existing study workflow — no six-week implementation project. A single 90-minute onboarding session is enough for most teams to put their first agent to work the same day, with your reviewers in the approval loop from hour one.
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.
eRIC AI agents work inside your existing study workflow — no six-week implementation project. A single 90-minute onboarding session is enough for most teams to put their first agent to work the same day, with your reviewers in the approval loop from hour one.
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.
eRIC AI agents work inside your existing study workflow — no six-week implementation project. A single 90-minute onboarding session is enough for most teams to put their first agent to work the same day, with your reviewers in the approval loop from hour one.
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
On-Time Recruitment
Countries
Trials
Patients
Repeat Business
On-Time Recruitment
Countries
Trials
Patients
Repeat Business
On-Time 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.