EryonCite

SaaS Solution for Automated Medical and Regulatory Review

EryonCite, a sovereign SaaS solution, is accessible on all devices and compatible with major browsers.

Designed to accelerate your reviews, it quickly detects regulatory and scientific non-compliances.

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Roadmap

In progress
1

Development

Now - September 2025

Creation of the SaaS platform and integration of sovereign AI.

2

Beta Testers

October 2025

Testing phase with our selected partners.

Become a tester
3

Public Launch

April 2026

Availability for all companies.

Thanks to its intelligent analysis engine, EryonCite

Identifies compliant and non-compliant content,
Identifies sections requiring human review (due to regulatory subjectivity),
Generates a structured report that reduces your review time by at least 50%.

A solution that enhances your reviews without replacing them.

A quick solution for all your verifications

Regulatory Review

Our regulatory review process relies on a rigorous approach, designed to meet the requirements of health authorities and your organization. It includes:

Complete verification of compliance with regulatory body rules
Verification of all embedded links and external citations
Application of internal rules specific to your company
Ensuring all disseminated information is up-to-date at the time of review

Medical Review

Our medical review ensures the scientific rigor of your documents and their compliance with good medical publishing practices. It includes:

Verification of the presence of reference medical indicators
Validation of the cited references
Highlighting references in scientific publications of your reference pack, according to ANSM standards
Verification of the presence and uniformity of the bibliography
Detection and highlighting of outdated, invalid, or inconsistent references

The benefits of automating with EryonCite

Manual reviews take up internal resources on repetitive tasks, a source of frustration and wasted time.

EryonCite automates compliance analysis, delivering an annotated document and a clear report, ready for validation.

The software integrates easily with your existing tools for smooth adoption by your teams:

RIM - Regulatory Information Management
QMS - Quality Management System
DMS - Document Management System
DAM - Digital Asset Management
Regulatory platforms

A Four-Step Method

  • 1

    Audit

    Initial audit with your teams to define internal standards and expected levels of compliance

  • 2

    Configuration

    Custom configuration of the solution according to your rules and processes

  • 3

    Training

    Quick training of your teams on the interface and operation

  • 4

    Supervision

    Continuous technical and functional monitoring, with responsive support and scalability

Types of Supported Documents

Promotional documents

Kakemonos, roll-up, banners
Medical visit presentations (ADV, eADV, pptx)
Promotional emails / campaigns
Scientific information dossiers (DIS)
Clinical cases
Dosage sheet
Press release / press statement
Script
Documents intended for healthcare professionals (HCP)
Website
Newsletters

Non-promotional documents

Documents intended for the general public
Documents intended for patients
Documents providing information on the pathology
Videos
Posters, flyers in pharmacies
Press, TV, radio advertisements
Social media publications
Product websites, QR codes

Digital content and campaigns

Digital content
Newsletters, banners, chatbot scripts
Texts for mobile apps, podcasts, educational videos

Cross-marketing and medical documents

Therapeutic education programs
Documents for patient associations
Co-creation with KOLs (Key Opinion Leaders)
FAQ templates, internal training documents
Supports for trade shows, congresses

Security and Regulatory Compliance

Our solution is designed to meet the following standards:

MDR (EU 2017/745)
ISO 13485
GMP / GxP
GDPR
ANSM / HAS
Your specific internal standards

Deliverables are adjusted to your validation processes, including your safety margins.

Data Confidentiality and Sovereignty

Ensured Confidentiality

Transfers via HTTPS, SFTP or encrypted drive
Optional anonymization

Sovereign Hosting

Servers in France (OVHcloud, Outscale, Scaleway)
Locally executed AI
TLS 1.2+, AES-256 encryption

GDPR Compliance

No health data processed
Secure deletion of files after delivery
GDPR clauses included in our T&Cs

Contractual Commitment

Systematic confidentiality agreements (NDA)
Segregation between client projects

Areas of Expertise

We mainly operate in two highly regulated sectors:

Pharmaceutical industry

Compliance with pharmaceutical regulations.

Medical devices

Specialized expertise in the regulatory requirements of medical devices.

Other regulated sectors

Eryon also adapts to other regulated sectors according to your specific needs.

Ready to optimize your reviews with EryonCite?

We offer you a test access or a personalized demonstration to evaluate the suitability of EryonCite to your use cases.

Test the solution