bout Tesserblu
Software for the work that brings medicines to patients.
Tesserblu builds Salvus — a governed-AI platform spanning clinical trials and pharmacovigilance. We believe AI should accelerate the most demanding work in life sciences without ever loosening the controls that keep it safe.
Why we exist
Drug development still runs on a patchwork of aging, document-heavy systems that don't talk to each other — and every handoff is a place where time is lost and risk creeps in. We think it should work as one governed system.
AI can change how this work gets done. But in a field where a single miscoded case or a broken audit trail has real consequences, speed without governance isn't progress — it's exposure.
Tesserblu exists to give clinical and safety teams one platform where AI does the heavy lifting, qualified people make every regulated decision, and every action is captured, compliant and inspection-ready. Fast and safe, at the same time.
What we build
One platform. Two suites. Twelve modules.
Salvus covers the drug-development lifecycle end to end. Every module shares one data model, one design system, one audit trail and one governed-AI framework — so teams can adopt a single module or the whole platform.
Clinical Trial · 4 modules
Run a study from protocol to lock.
CTMS, RTSM/IRT, CDMS and EDC — planning, randomization and supply, data management and electronic data capture, all on one operational source of truth.
Pharmacovigilance · 8 modules
Run the full safety lifecycle.
From case intake and ICSR processing through literature monitoring, signal detection, regulatory intelligence, risk management, materiovigilance and quality management.
What we believe
The principles the whole platform is built on.
AI proposes, people decide.
Human-in-the-loop is a design principle, not a setting you switch on. Every regulated decision — coding, causality, signals, data changes — passes a qualified human gate, with the AI's contribution logged.
One source of truth.
Fragmentation is the enemy of both speed and safety. A shared data model means information flows across the lifecycle without re-keying, reconciliation gaps or version drift.
If it isn't audit-trailed, it didn't happen.
Every action, suggestion and override is captured in an immutable, 21 CFR Part 11-ready trail. Compliance is built into the foundation, not bolted on before an inspection.
Built with the people who use it.
Designed by people who have done pharmacovigilance, clinical operations and regulatory work — for the reviewers, coders and managers who live inside these systems every day.
2
Suites — clinical & PV
12
Integrated modules
10+
Regulatory frameworks
1
Governed-AI framework
Who we are
Domain experts, building for domain experts.
Tesserblu brings together people from pharmacovigilance, clinical operations, regulatory affairs and applied AI. We've been the users of the tools we're replacing — which is why governance, auditability and the reviewer's day-to-day experience sit at the centre of everything we build, not the edges.
We're a focused team based in Bengaluru, working with sponsors, CROs and marketing-authorisation holders around the world.
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Founder & CEO
One-line bio — background, what they lead, and why this problem matters to them.
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Head of Product
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Head of Engineering
One-line bio — platform, applied AI and the governed-AI framework behind Salvus.