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● GenAI & Agentic-AI for Drug Development
One platform for the entire
drug development lifecycle.
Tesserblu builds Salvus — eleven integrated modules spanning clinical trials and pharmacovigilance. AI accelerates the work; humans stay in control; every action is audit-trailed and compliant.
Clinical Trial · 4
Pharmacovigilance · 7
📋
CTMS
Trial Planning
Sites
⇄
RTSM
Randomization
Sites
📄
EDC
eCRF
Part 11
🛡
CTMS
Trial Planning
Sites
11
Integrated modules
2
Suites — Clinical & PV
10+
Regulatory frameworks
1
Governed AI framework
The Salvus Platform
Eleven modules. Two suites. One source of truth.
Adopt one module or the whole platform. Everything shares a common data model, design system, audit trail, and governed-AI framework.
Clinical Trial Management System
CTMS
Salvus CTMS gives sponsors, CROs and sites a single operational truth across protocol management, site activation, participant tracking, milestone control, and regulatory submissio…
Protocol & Study Setup
Site Identification & Activation
Participant Tracking
Milestone Monitoring
Clinical Suite
Randomization & Trial Supply Management
RTSM / IRT
Salvus RTSM handles every complexity of modern trial supply: adaptive randomization, multi-depot inventory, blinded and unblinded role enforcement, expiry management and real-time …
Randomization Design Studio
Real-time Treatment Allocation
Blinding & Unblinding
IP Inventory & Expiry Management
Clinical Suite
Clinical Data Management System
CDMS
Salvus CDMS is the data management operations layer above the EDC: cross-study discrepancy analytics, DMP execution, coding, medical review listings and database lock governance. A…
Data Validation
Cross-Study Analytics
Medical Coding
Query Management
Clinical Suite
Electronic Data Capture
EDC
Salvus EDC combines a no-code form designer, a declarative edit-check engine with a built-in test harness, risk-based SDV and CDISC-standard exports — built so per-study validation…
eCRF Form Designer
Edit-Check Engine
Visit Schedule & Dynamics
Risk-Based SDV / SDR
Clinical Suite
See It in Action
Watch the platform work.
From randomization to signal detection — see how each module handles the workflows your team faces every day.
Browse product demos — click to switch
Clinical Trial Management System
CTMS · 3:45
Case Intake
Intake · 4:01
Regulatory Intelligence
Reg Intelligence · 3:22
Randomization & Trial Supply Manag
RTSM / IRT · 4:12
ICSR Case Processing
ICSR · 5:13
ICSR Case Processing
ICSR · 5:13
Clinical Data Management System
CTMS · 3:45
Literature Review & Monitoring
Crypta · 3:38
Electronic Data Capture
EDC · 2:54
Signal Detection & Management
Signum · 4:47
Qualitus
Qualitus · QMS · 3:15
Why one platform
GenAI that accelerates. Governance that protects.
Salvus applies AI where it saves the most time — drafting, extraction, coding, triage — while keeping regulated decisions in human hands.
Human-in-the-loop by design
AI proposes; qualified reviewers accept. Coding, causality, signal decisions and data changes all pass a human gate — with the AI's contribution logged.
Human-in-the-loop by design
AI proposes; qualified reviewers accept. Coding, causality, signal decisions and data changes all pass a human gate — with the AI's contribution logged.
Human-in-the-loop by design
AI proposes; qualified reviewers accept. Coding, causality, signal decisions and data changes all pass a human gate — with the AI's contribution logged.
Human-in-the-loop by design
AI proposes; qualified reviewers accept. Coding, causality, signal decisions and data changes all pass a human gate — with the AI's contribution logged.
Compliant with
US FDA
EU EMA / GVP
21 CFR Part 11
EU Annex 11
CDISC
ICH E2B(R3)
GAMP 5
Health Canada
PMDA
TGA · CDSCO
Swissmedic
See the whole platform in one demo.
Start a 21-day free trial — no credit card required.
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