EryonAgence

Augmented Medical and Scientific Review Solution

EryonAgence combines sovereign AI and human expertise to accelerate your medical and regulatory reviews, ensuring compliance and speed.

% of review time saved by your teams.
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All your verifications simplified

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
Validation of visual content (images, QR codes, logos, etc.) present in the document

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Detection and highlighting of outdated, invalid, or inconsistent references
Delivery of a clear, annotated document

Free up time for your teams

Proofreading tasks take up your teams on repetitive and time-consuming tasks, representing up to 50% of the working time of medical or regulatory marketing services. EryonAgence combines sovereign artificial intelligence with human expertise to provide you with a compliant document, accompanied by a detailed report ensuring quick and reliable verification.

We manage the back-and-forth between regulatory, marketing, and medical teams, freeing up your resources while leaving you with the final validation.

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
Videos

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

Areas of Expertise

We mainly operate in 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.

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

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

A Four-Step Method

  • 1

    Audit

    Audit of your company's needs

  • 2

    Transmission of your documents

    Submit your documents on our platform or via our secure and sovereign partner solution.

  • 3

    Analysis

    Two analyses are performed: one with artificial intelligence and then by a human reviewer.

  • 4

    Response within 48 hours

    Receive a detailed report within 48 hours allowing for quick validation by your teams.

What price?

Scientific Review

Verification of clinical data and creation of reference packages.

Average: €1,000/document

Regulatory Review

Compliance with defined standards post-audit.

Average: €1,000/document

Combined Review

Comprehensive approach (scientific + regulatory).

Average: €1,500/document

Turnaround Time

Delivery within 48 hours, with expert validation

(subject to prior assessment)

Detailed rates by document type

Document Type Scientific Review Regulatory Review Combined Review
Kakemono / roll-up / banner 100 – 200 € 100 – 200 € 200 – 400 €
Medical visit presentation (eADV / ADV) 500 – 1000 € 500 – 1000 € 1000 – 2000 €
Promotional email / campaign 100 – 200 € 100 – 200 € 200 – 400 €
Scientific Information Dossier (DIS) 500 – 1000 € 500 – 1000 € 1000 – 2000 €
Clinical case / product sheet / sales pitch 500 – 1000 € 500 – 1000 € 1000 – 2000 €
Non-promotional document 500 – 1000 € 500 – 1000 € 1000 – 2000 €
Poster / flyer / QR code 100 – 200 € 100 – 200 € 200 – 400 €
Marketing video / social media 500 – 1000 € 500 – 1000 € 1000 – 2000 €
SEO content / product website / SEA 200 – 1000 € 200 – 1000 € 400 – 2000 €
Newsletter / chatbot / app / podcast 100 – 200 € 100 – 200 € 200 – 400 €
Educational program / FAQ / training 200 – 1000 € 200 – 1000 € 400 – 2000 €

Ready to accelerate your reviews with EryonAgence?

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