One platform for the institutions healthcare depends on.
We serve government health agencies and large commercial pharma and hospital enterprises — bridging raw, fragmented data and the decisions their people have to act on and defend. Each area below starts as a single work package with a measurable outcome, built from modules that already exist.
Market access & HEOR
The evidence already exists. The cost is re-assembling it for every market, payer, and format. One governed evidence base generates value dossiers, HTA submissions, and local value stories on demand — built for global and regional market access, HEOR, medical affairs, and local affiliate teams.
Proof: a global pharma reused one knowledge base across 8 APAC markets — dossier creation moved from weeks to days.
Read the full breakdown →Clinical trials
Recruitment fails on eligibility, not intent. Structured and unstructured records hold the answer, but they sit inside the site's walls — where the AI has to go. Built for clinical development, trial operations, feasibility, and data science teams, with academic and hospital study sites.
Proof: a top-5 pharma intermediate-AMD study targets 2× the historical screen rate with GDPR-compliant, site-resident data.
Read the full breakdown →Supply chain & hospital operations
High-cost, short-shelf-life inventory managed in spreadsheets between systems that never agreed on a unit of measure. The platform unifies the data, forecasts demand, and explains every order it proposes. Non-clinical operations only — no diagnosis, no treatment decisions. The same modules run outside healthcare too: medtech distribution, manufacturing, and public-sector procurement.
Proof: a public hospital oncology pharmacy runs the full chain, built entirely from registered, reusable tools.
Read the full breakdown →Government & regulators
Regulators carry rising submission volume with fixed headcount, and cannot send a single document to a public model. The workflow has to run inside government cloud — built for health authorities, regulatory agencies, and public health bodies.
Proof: live in Singapore's Government Commercial Cloud, extended one work package at a time on shared modules.
Read the full breakdown →Regulatory document automation
Every submission starts as a document problem before it's a compliance problem. The same extraction, compliance-check, and audit-trail modules that run inside a regulator's cloud also run on the sponsor side — built for regulatory affairs, medical writing, and labelling teams at pharma and biotech sponsors.
Proof: the same registered modules already run inside Singapore's Government Commercial Cloud, on the regulator's side of the same transaction.
Read the full breakdown →Not sure which work package to start with? That is the first conversation.
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ECLYPSE
AI
Our proprietary AI orchestration platform for healthcare: one engine, a registry of reusable task modules and domain agents, and a governed knowledge base — deployed inside your walls and run by your team.