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Clinical Trial Suite · 4 Modules
Run the whole trial on one source of truth.
Four integrated modules — CTMS, RTSM/IRT, CDMS and EDC — spanning planning to database lock. Governed AI accelerates the work; qualified humans stay in control; every action is audit-trailed and compliant.
4
Modules
1
Data model
6+
GCP frameworks
100%
Audit-trailed
CT-01
CTMS
Trial Management
CT-02
RTSM
Randomization & supply
CT-03
CDMS
Data Management
CT-04
EDC
Electronic Data Capture
One platform · one design system · one audit trail
47
Active studies
312
Sites managed
18,400
Participants
94%
Milestone on-time
The modules
Four modules. One connected trial.
Adopt one module or the whole suite. Everything shares a common data model, design system, audit trail and governed-AI framework.
CT-01
CTMS
Clinical Trial Management System
Orchestrate every study phase — from first site to database lock.
A single operational truth across protocol management, site activation, participant tracking, milestone control and regulatory submission coordination. AI-assisted planning flags at-risk milestones up to eight weeks before they slip.
Protocol Setup
Site Activation
Participant Tracking
Milestone Monitoring
CT-02
RTSM
Randomization & Trial Supply Management (IRT)
Every complexity of modern trial supply — under one blinded roof.
Adaptive randomization, multi-depot inventory, blinded and unblinded role enforcement, expiry management and real-time resupply — with strict separation of duties and a full accountability trail.
Adaptive Randomization
IP Dispensing
Blinding / Unblinding
Depot Inventory
CT-01
CDMS
Clinical Data Management System
The data-management operations layer above your EDC.
Cross-study discrepancy analytics, data-management-plan execution, medical coding, medical review listings and database-lock governance — so clean data and a defensible lock are the default, not a scramble.
Discrepancy Analytics
Medical Coding
Medical Review
Database Lock
CT-04
EDC
Electronic Data Capture
No-code forms, declarative edit checks, faster builds.
A no-code form designer, a declarative edit-check engine with a built-in test harness, risk-based source-data verification and CDISC-standard exports — built so per-study validation is fast and inspection-ready.
No-code eCRF Builder
Edit Checks
Risk-based SDV
CDISC Export
See it in action
Watch each module work.
From randomization to database lock — short, guided walkthroughs of the workflows your clinical teams face every day. Click any card to play.
CTMS
CT-01 · Demo
Clinical Trial Management System
CT-02 · Demo
Randomization & Trial Supply
CT-03 · Demo
Clinical Data Management System
EDC
CT-04 · Demo
Electronic Data Capture
Why one platform
GenAI that accelerates. Governance that protects.
Salvus applies AI where it saves the most time — drafting, extraction, planning, reconciliation — while keeping every regulated decision in qualified human hands.
01
Human-in-the-loop by design
AI proposes; qualified reviewers accept. Coding, data changes and milestone actions all pass a human gate — with the AI's contribution logged.
02
Audit-trailed by default
Every action, every AI suggestion and every override is captured in an immutable, 21 CFR Part 11-ready trail — inspection export in one click.
03
One data model
Modules share a common data model, so protocol, supply, capture and lock data flow across the trial without re-keying or reconciliation gaps.
04
Deploy one or all
Adopt a single module standalone, or run the whole suite. Each stands on its own — and gets stronger when connected to the rest.
Built for inspection
Compliant with the frameworks
your auditors expect.
ICH E6(R3) GCP
ICH E8(R1)
21 CFR Part 11
EU Annex 11
CDISC / CDASH
GAMP 5
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