Sovereign, fast, and secure medical and regulatory review.

Accelerate your reviews with Eryon, the French solution dedicated to the health industries.

Our Solutions

EryonAgence

Turnkey outsourced service

Validation of citations and references
Verification of regulatory compliance
Document update control
Comprehensive analysis of the entire document
Compliance with your editorial guidelines
Precise response within 48 hours
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EryonCite

Sovereign SaaS platform

Real-time automated analysis
Detection of non-compliances
Automatic structured report
Integration with your existing tools
Training and support
Transparency of results
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Our trusted partners

They support us

Why Choose Eryon?

Full traceability

Each correction is documented, justified, and archived.

Hybrid review

Sovereign artificial intelligence is coupled with expert human reviewers.

Data sovereignty

Data is hosted in France on secure servers, without extra-European dependency.

Time saving

Over 50% of time is saved on your reviews.

Guaranteed compliance

Constant alignment is ensured with scientific and regulatory benchmarks (EMA, ANSM, etc.).

Full transparency

Artificial intelligence is used with full clarity, security, and traceability.

Supported Documents

Send us your documents: PDF, Word, PowerPoint, images... Our platform adapts to your work habits. Format not listed? No problem.

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PDF
Word
Image
PowerPoint

Who is Eryon for?

Eryon is designed for professionals in highly regulated sectors, facing frequent, lengthy, and critical reviews.

We support

Pharmaceutical companies
Medical device companies
Cosmetic companies

Target Profiles

Medical Managers
Regulatory Managers
Product Managers
Managers and Executives

, Gabin

Inconsistencies Between EUDAMED, CER, PSUR, and Technical Files: A Growing Risk in 2026

In 2026, inconsistencies between EUDAMED, CER, PSUR, and technical files pose an increasing risk for medical device manufacturers. Learn how to anticipate and address these discrepancies.

Read the article

, Gabin

EUDAMED in 2026: Concrete Obligations for Medical Device Manufacturers

In 2026, EUDAMED becomes mandatory for medical device manufacturers. What are the concrete obligations regarding traceability, consistency, and data updates?

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, Gabin

Health Data and Sovereignty: Why We Reject Non-European Clouds

Health data and sovereignty: why entrust your strategic documents to European clouds? GDPR, security, and local solutions explained.

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Do you want regulatory compliance?

We offer you an evaluation of the compliance of your documents to European regulation standards.

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