EryonAgence

Augmented Medical and Regulatory 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Detection and highlighting of outdated, invalid, or inconsistent references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.