We support
Pharmaceutical companies
Medical device companies
Cosmetic companies
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
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
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.
Contact Us
PDF
Word
Image
PowerPoint
Who is Eryon for?
Eryon is designed for professionals in highly regulated sectors, facing frequent, lengthy, and critical reviews.
Target Profiles
Medical Managers
Regulatory Managers
Product Managers
Managers and Executives
, Gabin
What Is the Required Frequency for Updating Technical Files in 2026 to Stay MDR-Compliant?
In 2026, what is the required frequency for updating technical files to stay compliant with MDR? Discover the triggering events and best practices for continuous compliance.
, 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.
, 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?
Do you want regulatory compliance?
We offer you an evaluation of the compliance of your documents to European regulation standards.
Contact Us