Eclypse AI
Solutions

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 Clinical trials Supply chain & operations Government & regulators Regulatory document automation
Agent HERO

Find the agents built for your work.

Agent HERO is a suite of domain agents, grounded in MeSI, that cover the institutions below from early development through post-market. Pick who you are — the relevant agents and benefits follow.

  • Faster evidence generation: HEOR and medical affairs agents turn literature and real-world data into submission- and launch-ready evidence, grounded in MeSI.
  • One evidence base, every function: medical affairs, HEOR, regulatory, and commercial teams work from the same governed knowledge base instead of five siloed searches.
  • Earlier signal visibility: the pharmacovigilance agent surfaces emerging safety signals continuously, not just at periodic review.
  • Less assembly, more judgment: your experts review and approve agent-drafted outputs instead of building them from scratch.
01
Discovery & Development
regulatory_agentmedical_affairs_agent

Early regulatory precedent and literature landscaping, so strategy is grounded before protocols are locked.

02
Clinical / Pre-market Evidence
heor_agentmedical_affairs_agent

Evidence planning, economic model groundwork, and trial-related medical and scientific response.

03
Regulatory Submission & Review
regulatory_agentheor_agent

Dossier assembly, compliance checks, and HTA/payer submissions built from the same evidence base.

04
Launch & Commercialization
commercial_agentheor_agent

Launch materials and localized value dossiers, generated market by market.

05
Post-Market & Surveillance
pharmacovigilance_agentmedical_affairs_agent

Continuous signal detection and ongoing scientific response, not periodic batch review.

  • Pathway clarity early: the regulatory agent surfaces comparable clearances and predicate pathways before you commit to a submission strategy.
  • Submission-ready documentation: dossier assembly and compliance-check modules reduce the manual burden of 510(k)/PMA/CE-mark preparation.
  • Reimbursement evidence, not just clinical evidence: the HEOR agent builds the economic case alongside the clinical one.
  • Continuous vigilance: post-market complaint and adverse-event trends are monitored continuously, not reviewed in batches.
01
Discovery & Development
regulatory_agentmedical_affairs_agent

Predicate device and pathway scanning alongside clinical literature for design inputs.

02
Clinical / Pre-market Evidence
heor_agentmedical_affairs_agent

Economic modelling for reimbursement coding and clinical evaluation report support.

03
Regulatory Submission & Review
regulatory_agent

510(k), PMA, and CE-mark dossier assembly against the standards that actually apply.

04
Launch & Commercialization
commercial_agentheor_agent

Launch collateral and payer value stories, so reimbursement isn't an afterthought.

05
Post-Market & Surveillance
pharmacovigilance_agent

Complaint and adverse-event trend monitoring for post-market surveillance reporting.

  • Horizon scanning and benchmarking: how comparable agencies in other markets have assessed or reimbursed the same technology.
  • Evidence review support: faster, traceable summaries of clinical and real-world evidence.
  • Consistency: a clearer view of the dossier standards manufacturers face across markets, which can raise the quality of what reaches you.
  • Capacity: less routine effort, so scarce expert time goes to judgment.
01
Discovery & Development
regulatory_agent

Horizon scanning of emerging technologies and how comparable agencies elsewhere have assessed them.

02
Clinical / Pre-market Evidence
regulatory_agentheor_agent

Faster, traceable summaries of the clinical and real-world evidence submitted to you.

03
Regulatory Submission & Review
regulatory_agent

A clearer, more consistent view of the dossier standards manufacturers face across markets.

04
Launch & Commercialization
regulatory_agent

Post-authorization commitment tracking and label/claims compliance monitoring.

05
Post-Market & Surveillance
pharmacovigilance_agent

Safety-signal and real-world evidence review, with less routine effort spent on triage.

All agents are grounded in MeSI, Eclypse's quality-gated evidence base. Learn more about Agent HERO →

01

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.

Economic modelling specifically runs through Agent HERO, grounded in MeSI's evidence base.

Read the full breakdown →
02

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 →
03

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 →
04

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 →
05

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.

Book a working session
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.

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