eRIC SOLUTIONS, is a full-service CRO and regulatory affairs partner. We run Phase I–IV clinical trials and the data, biostatistics, safety, and regulatory work behind them — for pharma, biotech, and medical-device sponsors in the US, Europe, and Asia. Our eRIC AI agents remove the operational bottlenecks that slow trials down, with humans in control.
eRIC SOLUTIONS, is a full-service CRO and regulatory affairs partner. We run Phase I–IV clinical trials and the data, biostatistics, safety, and regulatory work behind them — for pharma, biotech, and medical-device sponsors in the US, Europe, and Asia. Our Eric AI agents remove the operational bottlenecks that slow trials down, with humans in control.
From protocol design to analysis-ready data, eRIC AI applies artificial intelligence deliberately to remove operational bottlenecks — with humans firmly in control. Seven agents cover database design, data entry, monitoring, statistics, medical writing, document management, and project management. eRIC AI is live now.
Trials
Patients
Repeat Business
Recruitment
Countries
Trials
Patients
Repeat Business
Recruitment
Countries
Trials
Patients
Repeat Business
Recruitment
Countries
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 customization, 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 customization, 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 customization, 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.
We run early-phase oncology and complex trials end to end and know exactly where they slow down.
eRIC AI removes repetitive work while a person approves every output.
Every line item documented; pass-throughs at actuals, 0% mark-up.
19 days DB design
19 days — database design complete (USA, 4 sites, 60 subjects).
5 wks to first site
Within 5 weeks of signing — first site initiated.
faster startup
27% faster than the industry average.
Tell us the protocol, the phase, and the timeline. We will come back with a fixed-fee proposal and a team that has run trials like yours.