Simplify your documentation compliance
AI-powered regulatory review for pharma and medical devices. Self-service, with our experts, or integrated into your processes · hosted in France.
The EryonOne journey, end to end
From sign-in to annotated report delivery.
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 four angles: regulatory, scientific, linguistic, formatting.
Regulatory review
Cross-check against applicable texts (MDR, IVDR, GVP, GMP, AI Act, HDS) 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.
Four solutions, a single engine
Whether you have a one-off file to verify or a full regulatory department to equip, we have a suitable offering.
One file, one analysis. No subscription, no commitment. Ideal for a one-off submission.
Available nowOur Regulatory & Quality Affairs experts + our AI, deployed in 48 h on your file. Documented deliverables, ready to submit.
Regulatory architecture, documentation strategy, AI integration into your quality IS.
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.
Risk analysis
Map of regulatory and scientific risk points across your whole file.
EUDAMED check
Consistency check between your EUDAMED declarations and your technical file. Detection of CER / PSUR inconsistencies.
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, or external references (ISO standards, FDA / ANSM guidances).
Background research
Background and scientific reference search directly on PubMed, Google Scholar and your internal bases.
Four steps, whatever your flow
Whether it's a one-off file, ongoing watch or a team project, the journey stays the same — you steer, Eryon assists.
Import
Upload your documents (Word, PDF, XML), in project or one-off mode. Strict isolation per client and per project.
Analyse
The AI cross-references (regulatory, scientific, internal) and identifies gaps, omissions and risks.
Review
Each suggestion comes with its justification. You accept, edit or reject. The final decision stays human.
Export
Corrected documents, audit trail and report (Word, PDF or structured export), ready to archive or submit.
Your documents never leave France
Our offerings rely on sovereign French infrastructure qualified by ANSSI. Sovereign open-source models. Every request, every log, every vector stays in France.
Sovereign cloud · ANSSI
ANSSI-qualified, Outscale hosting (Dassault).
GDPR native
Strict isolation, right to erasure, on-demand export.
Open-source models
Models hosted and served in Europe.
Audit trail
Every suggestion, every decision, journaled.
SSO & SCIM
Native integration with your IDP (Okta, Entra, Keycloak).
They trust us
« On a file that evolves over months, with constant updates, you eventually stop seeing contradictions. Having an external, automated eye is a game-changer. »