QCD Visual Pro · Clinical Trial Data Intelligence

See your trial.
Decide with confidence.

QCD Visual Pro is the clinical-data workbench for sponsors, CROs, and clin-ops teams. Stand up an audit-ready dashboard the same week your data lands — patient-level detail, Part-11 sign-off, AI assistant on every chart.

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 holds the answers.
They're buried in PDFs and CSVs.

QCD Visual Pro surfaces them — in clicks, not sprints.

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 on full trial datasets
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
Patient Profile · Swim Lane

The full life of a subject, in one view.

QCD Visual Pro renders every patient as a swim lane that aligns dosing, visits, adverse events and concomitant medications on a single study-day axis. Click any segment for the source record. Click a subject for the full narrative.

One row per subject, every protocol event aligned
AE severity, CM indication, dose modifications — colored
One click from cohort trend to individual narrative
Patient Profile — Combined Timeline
5 subjects · Day -14 → 365
C1D1 103-7001 103-7002 109-7019 111-7011 120-7036 Day 0 90 180 270 365 Treatment Con-Meds G1 G2 G3 G4/SAE

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 every subject in your study without leaving the browser. Your data team ships answers in minutes, not sprints.

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 — same vocabulary, same UX — from a first-in-human safety study through pivotal trials and registry-scale post-market work.

Decisions at the speed of trust

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

25+
Pre-built clinical dashboards
<2s
Median chart render time
I–IV
All trial phases supported
21 CFR 11
Audit-ready sign-off trail

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.