Clinical Trial Data Intelligence

See your trial.
Decide with confidence.

Patient-level intelligence, sponsor-grade trust. Turn locked study data into answers your team can act on — without the wait, without the spreadsheet wars.

Adverse Events by System Organ Class
Live n=12,847
GI
CNS
CV
Derm
Resp
Endo
Hem
Built for sponsors, CROs & biotech teams
Phase I–IV CDISC Ready 21 CFR Part 11 GxP Aligned SDTM & ADaM

Your trial generates millions of data points.
Most of them sit in PDFs.

We change that. In seconds.

Real-time trial intelligence

Every patient, every endpoint, in one beautiful view.

Stop waiting for your data team's next deliverable. Filter by site, arm, dose, or any covariate — your dashboards update instantly. Insights that used to take a sprint now take a sip of coffee.

Sub-second filters across millions of records
Drag, drop, decide — no SQL required
Always synced with the source of truth
Kaplan–Meier Survival
Study 2026-A
Treatment Placebo
Audit-ready by design

Every click, logged. Every dataset, lineage-tracked.

Built from the ground up for regulated environments. Full audit trails, versioned datasets, and provenance you can hand to a regulator without breaking a sweat.

21 CFR Part 11 aligned
CDISC SDTM & ADaM native
Tamper-evident snapshots for every export
Subgroup Hazard Ratios
95% CI
HR = 1.0 Overall Age < 65 Age ≥ 65 Female Male High biomarker Low biomarker 0.5 2.0

Everything your trial team needs.
Nothing it doesn't.

From data ingestion to regulatory export — one platform, every phase.

Real-time intelligence

Filter, slice, and explore millions of patient records in milliseconds. Your data team becomes 10x faster — without hiring anyone.

Audit-ready by design

Provenance, lineage, and versioning baked into every dataset. Regulators love it. So do your QA leads.

Patient-level transparency

Drill from a population trend to a single subject narrative in two clicks. Zero context loss.

Drag, drop, decide

If you can use a spreadsheet, you can build a publication-grade visualization. No SQL, no Python, no waiting.

Phase I → post-market

One platform that scales from a 30-patient FIH study to a 30,000-patient registry. Same vocabulary, same UX.

Decisions at the speed of trust

Daily DSMB-ready outputs. Sites that flag themselves. Endpoint signals you'd otherwise miss until lock.

0M+
Patient records analyzed
<2s
Median query time
0%
Faster than spreadsheets
I–IV
All trial phases

Ready to see your trial
in a new light?

Book a 20-minute walkthrough with our team. Bring your own data — we'll load it in front of you.