The bridge between clinical activities & digital success
A unified platform where patients, sites, sponsors, and partners connect and collaborate in a real-time, compliant environment — from first visit to database lock.
21 CFR Part 11 · just now
Every stage of the trial, in one connected system
Start with a single module and scale as you grow. No double data entry, no silos — every product shares one source of truth.
EDC Software
Capture and manage clinical data with real-time edit checks, version control, and an immutable audit trail.
Explore EDCCTMS
Gain visibility into every site, milestone, and budget line across your entire trial portfolio.
Explore CTMSRTSM / IWRS
Randomization and trial supply management that keeps subjects enrolled and depots stocked.
Explore RTSMAuto-code adverse events against MedDRA and WHO-DD dictionaries in seconds — with human-in-the-loop review for every suggestion.
See how it workseCOA & PSP
Patient-reported outcomes and adherence tracking, mobile-first and multilingual.
Explore eCOABuilt for compliance, designed for speed
Replace fragmented, paper-heavy workflows with one defensible system of record — and get your first study live in under two weeks.
Live in under 2 weeks
Our onboarding team handles study build and configuration so your team can focus on research.
Compliance by design
Immutable audit trails and hash-chain tamper evidence on every data touchpoint.
Built for the region
Decree 13/2023 compliance, Vietnamese-language support, and local regulatory context.
Defensible by default
Every record is built to stand up to inspection — regulatory compliance isn't a checkbox, it's baked into the architecture.
"The best quality of ClinicalDataS EDC is how user-friendly it is for sites to enter data — we reached our first monitoring visit with zero data discrepancies."
Ready to see how ClinicalDataS makes the complex easy?
Join 50+ clinical teams who've made the switch. We'll get your first study live in under two weeks.