Specialized AI · Healthcare · Compliance

Simplify your documentation compliance

AI-powered regulatory review for pharma and medical devices. Self-service, with our experts, or integrated into your processes · platform hosted in France.

Specialized AI Healthcare Compliance
01 Complete journey

The EryonOne journey, end to end

From sign-in to annotated report delivery.

02 What Eryon detects

An expert eye on every document, to free your experts from repetitive tasks

Files keep growing, requirements keep evolving. After many reads, some errors become invisible. Eryon re-reads under five angles: regulatory, scientific, formatting, linguistic, consistency.

Regulatory review

Cross-check against applicable texts (MDR, IVDR, ANSM doctrine, French Public Health Code…) and your internal references. Each gap is located down to the paragraph and justified by its legal basis.

Scientific review

Consistency check on data, figures, units, and cross-referencing with scientific literature (PubMed, Google Scholar, your internal sources).

Linguistic review

Spelling, grammar, regulatory terminology, multilingual translation consistency, readability.

Formatting review

Document structure, numbering, layout, eCTD/DITA template compliance, completeness of mandatory sections.

Additional features designed for your projects

Whether you're fixing a one-off file or running a continuous watch, Eryon adapts to your workflow.

Inconsistency review

Multi-document cross-analysis: leaflets, technical files, clinical reports. Each contradiction is located and qualified.

Tracked corrections

Every suggestion is timestamped, justified and auditable. The expert keeps the final say.

Edit suggestions

Rewordings backed by a legal text or scientific source. Accept, edit or reject in one click.

Internal consistency

The same fact stated differently in two places of the document is flagged, with both passages quoted.

Sourced scientific review

Each claim is checked against the references you upload: sourced, approximate, contradicted or not demonstrated.

Regulatory watch

Continuous tracking of your files against evolving applicable texts (MDR, IVDR, AI Act). Alerts on impact.

Internal & external references

Analysis against your SOPs, your templates and your charters, on top of the public texts we cover.

Background research

Background and scientific reference search directly on PubMed, Google Scholar and your internal bases.

04 How it works

Four steps, and you keep the call

Whether it's a one-off file, ongoing watch or a team project, the journey stays the same: you steer, Eryon assists.

1

You upload

Upload your documents, in project or one-off mode. Strict isolation per client and per project.

2

Eryon analyses

The AI cross-references (regulatory, scientific, internal) and identifies gaps, omissions and risks.

3

You arbitrate

Each suggestion comes with its justification. You accept, edit or reject. The final decision stays human.

4

You export

Annotated report, logged decisions and exports ready to archive or submit.

05 Security

Your documents, under control

EryonOne is hosted in France, in Roubaix, on a SecNumCloud-qualified OVHcloud offer. AI analysis runs on several models: Claude, GPT or Mistral, or your own access. Your documents never train a model.

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SecNumCloud-qualified

OVHcloud hosting in Roubaix, on an ANSSI-qualified offer.

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GDPR native

Strict isolation, right to erasure, on-demand export.

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Your choice of AI

Claude, GPT or Mistral as needed, or your own provider, a European model or one deployed on your premises.

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Audit trail

Every suggestion, every decision, journaled.

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No training

Your documents never train a model, neither at Eryon nor at the AI provider.

They support us

EuraTechnologies Eurasanté 3DS Outscale Bpifrance French Tech Lille Hauts-de-France Region OVHcloud Startup Program EuraTechnologies Eurasanté 3DS Outscale Bpifrance French Tech Lille Hauts-de-France Region OVHcloud Startup Program
“On a file that evolves over months, with constant updates, you eventually stop seeing contradictions. Having an external, automated eye is a game-changer.”
Frequently asked questions

Your questions about Eryon

Who is Eryon for?
For regulatory, scientific, marketing and medical leads in healthcare industries: pharmaceutical labs, medical device makers, biotechs, specialized agencies.
Which documents can Eryon work on?
Leaflets, technical files (MDR, IVDR), clinical reports (CER, PSUR), investigator brochures, promotional materials, SOPs. Any long, structured document held to specific requirements.
Is my data secure?
Yes. EryonOne is hosted in France, in Roubaix, on a SecNumCloud-qualified OVHcloud offer, with encrypted exchanges and per-account isolation. AI analysis runs on several models (Claude, GPT or Mistral) chosen for the document; depending on your requirements, it can use your own access, a European model or a model deployed on your premises. No document is shared with other users or used to train a model.
Does AI replace my experts?
No. Eryon handles cross-reading, consistency check and formatting. The final decision stays with your teams. Humans keep control.
What is the pricing model?
Three options: per-document fee or review packs (EryonAgence), per review, credit packs or subscription (EryonOne), consulting engagement (EryonConsult). The EryonOne price list is online, with an estimator.
How do I get started?
A 30-minute demo to understand your current flow, then a test on a sample document. No commitment.

Tell us how you review today

We'll show you how Eryon fits in.

Welcome offer

Your first review is free

Create your EryonOne account and upload your first document: the quote shows “free” and no credits are deducted.

Offer valid for every new EryonOne account, to be used within 30 days; a reminder is sent 5 days before it expires. No commitment: the reviews that follow show their price before every launch.