Your study, our engine.
When you're the sponsor of your own research, Evidilya gives you the CRO capabilities, à la carte, to design it, run it and publish it, without building a team from scratch. Designed specifically for PIs across hospitals, territorial care, pharmacies and home settings.
An à la carte menu, pick only what you need.
Every module can be commissioned on its own or combined into a full package. Scope, deliverables and budget are agreed in a Statement of Work, no funding or regulatory outcome is implied.
Protocol & scientific writing
Turn your idea into a rigorous, regulator-ready protocol, with the endpoints and rationale reviewers expect.
Biostatistics & SAP
Sample size, statistical analysis plan and analysis, independent, CDISC-standard, defensible.
Data management & EDC on ECS®
eCRF, ePRO (LucaH®) and a validated database, one source of truth, from first entry to lock. Build your eCRF in full autonomy, with validation rules, laboratory ranges and live preview, and open sites from day one without technical intervention.
Monitoring & quality (RBQM)
Right-sized on-site and remote monitoring against a risk plan, with ISO 9001 quality across the lifecycle.
Regulatory & ethics submissions
Dossier preparation and submission to ethics committees / competent authorities, hands-on support end-to-end.
Pharmacovigilance & safety
Adverse-event handling and safety reporting for your study, tuned to product class and jurisdiction.
Medical writing & publication
Study report, manuscript, abstract and lay-summary support, carry the evidence forward.
ECS® licence (tech-only)
If you only need the technology, licence ECS® and run the study on your own team.
From idea to publication, one partner, one SoW.
- Step 01
Tell us your study idea
A 30-minute call to understand your question, population and setting.
- Step 02
We scope the à la carte package
You pick the services you need, we propose scope, timeline and a transparent budget.
- Step 03
We set up and support
Protocol, EDC on ECS®, submissions, monitoring, PV, under one Statement of Work.
- Step 04
You publish
We take you through to report, manuscript and lay summary. You stay the PI-sponsor throughout.
Note: scope and support are agreed in a Statement of Work. Evidilya acts as your service and support partner, the PI remains the sponsor of the study, and our commitment is to evidence built to withstand regulatory and peer review.
Discuss your ISS with us.
A short call is enough for us to understand your study and shape the à la carte package.