Run modern studies with less friction.
Join Evidilya's investigator and site network. Phygital design keeps patients close to trusted care, while ECS® removes the busywork from data capture and monitoring.
Already running a study with us? Sign in to ECS®
Need help signing in?Hospital departments, community practices and pharmacies all run studies with us — interventional, observational and post-market, across cardiometabolic, oncology and immunology, digestive health and nutrition, neurology and mental health.
You are the sponsor. We are your CRO engine.
For Principal Investigators (PIs), academic groups and clinicians running their own study: pick only the CRO services you need, from protocol writing and EC/IRB submission to ECS® eCRF, monitoring, biostatistics and publication support. Fixed-scope, transparent, à la carte.
Your study, published.
Medical writing, statistical reporting and submission support take the work through to manuscript, abstract and lay summary. You stay the author and the sponsor; we do the work that usually stalls a good study after the last visit.
A partnership in the science, both ways.
Studies in your therapeutic area
Sponsor programmes come to us across cardiometabolic, oncology and immunology, digestive health and nutrition, neurology and mental health. When one fits your practice and your patients, you are on the list we call.
A named study manager who knows the science
One person who has read the protocol, understands the endpoints and answers you directly, from feasibility through database lock.
Data you can use
Your site's data stays visible to you in ECS® in real time, in structured, analysable form, within the access rules agreed with the sponsor.
Support through to publication
Medical writing and biostatistics carry the work to manuscript, abstract and lay summary. You stay the author.
Less administrative load
eCRF, eSource and eSDV reduce manual entry and reconciliation, and fewer disruptive on-site monitoring visits.
Direct-to-Participant, investigator-supervised
D-T-P extends your site: remote eConsent, televisits and home visits run under your oversight via ViSA, with LucaH® keeping participants informed and retained.
Configuration in full autonomy, control at the centre
Your site manages enrolment and per-centre progress on its own, with real-time data and no technical waits.
Become an Evidilya site or investigator.
Tell us about your site, your therapeutic focus and your patient population.
A partner in the science.
Run studies where the evidence lives.
One connected network across hospitals, territorial HCPs, pharmacies and home settings.