KOŚA for CROs & Clinical Research

One platform. Every protocol. Every site.Sponsor-ready, inspection-ready, always.

Stop stitching together paper, email and legacy eTMF systems. KOŚA runs every study on a single, audit-ready platform — so monitors, sponsors and regulators get what they need, when they need it.

Multi-site by design

One CRO. Many studies. Dozens of sites. Zero drift.

Every study gets its own scoped workspace — SOPs, training curricula, deviations and site files — while your central team maintains oversight across the portfolio.

Study portfolio on KOŚA

Oncology Study 301

12 sites

Cardiology Study 204

8 sites

Rare Disease Study 105

24 sites

Outcomes

What changes for your CRO the day you go live.

KOŚA replaces fragmented paper, email and legacy eTMF systems with one validated platform — designed by compliance architects who’ve passed sponsor and regulator audits.

See KOŚA running your study portfolio.

45-minute demo with a compliance architect — bring a real protocol, we’ll show you the study workspace in action.