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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…
Clinical Suite
Trial Planning
Site Management
Participant Tracking
Milestones
IMP Supply
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
IP dispensing
blinding/unblinding
Dispensing
Blinding/Unblinding
Randomization
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…
Clinical Suite
Trial Planning
Query Resolution
CDISC / CDASH
Data Lock
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…
Clinical Suite
eCRF Builder
Edit Checks
21 CFR Part 11
Audit Trail
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
Screenshot 2026-07-14 194753.png
Clinical Trial Management System
CTMS · 3:45
​Case Intake
Intake · 4:01
Screenshot 2026-07-14 195253.png
Regulatory Intelligence
Reg Intelligence · 3:22
Screenshot 2026-07-14 195457.png
Screenshot 2026-07-14 195136.png
ICSR Case Processing
ICSR · 5:13
Screenshot 2026-07-14 194641.png
Screenshot 2026-07-14 194856.png
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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