Privacy AI
Regulatory

Health data compliance, handled.

Tell us what you need. We'll tell you what it takes and how long, before you commit.

Contact us

Summary

Contact us

We are delighted to share that the ICM - Institut du Cancer de Montpellier was authorized by the French Data Protection Authority (CNIL) to conduct APAD-ECO study.

The CNIL granted authorization to conduct a medico-economic study on the effects of physical activity in women treated for breast cancer on April, 19th. This groundbreaking study involves combining data from two clinical trials with that of the Caisse nationale de l’Assurance Maladie, covering the period from 2009 to 2022.

The study aims to assess the long-term impacts of physical activity in patients who have undergone treatment for breast cancer.

We are proud to have contributed to this project by providing the ICM - Institut du Cancer de Montpellier with a compliant Data Protection Impact Assessment (DPIA), a crucial step in obtaining CNIL approval.

Contact us

FAQs

Our frequently questions

No items found.

Find out how iliomad can help your company.

[Map placeholder]
Only visible in production
38.709099
-39.182035
1.6
6d17042a3425c5b3
Your message has been received!
We'll get back to you as soon as possible.
Something went wrong, please try again.
Home

Discover our latest articles

View All Blog Posts
Abstract digital network connecting hospital icons, AI circuit patterns and GDPR shield symbols on a dark blue background, representing healthcare data protection themes
October 28, 2026
Healthtech
Data Breach & Cybersecurity
GDPR
Regulation
LLMS

Healthcare AI Agents, Vendor Breaches and GDPR Reforms: Weekly Privacy and Regulation Digest

This week's digest covers autonomous AI agent risks, a wave of US healthcare vendor breaches, the EU Digital Omnibus GDPR mandate and Swiss voice-biometric enforcement.

Clinical study protocol open on a desk beside a GDPR compliance checklist and a stethoscope, representing data protection obligations in clinical research
October 26, 2026
GDPR
DPIA
Health Data Strategy
Regulations & Guidelines
Regulation

Clinical study protocol data protection: a practical guide for sponsors

Learn how to embed GDPR-compliant data protection into your clinical study protocol. Practical guidance on Section 13, DPIAs, transfers and local formalities.

A researcher reviews a clinical site agreement alongside export control documentation for cross-border data transfer compliance
October 23, 2026
Regulations & Guidelines
Clinical Trials
Regulation
Consent Forms
Big Data

Clinical Site Agreement: Navigating US Export Control Review of Cross-Border Data Transfers in Clinical Trials

Learn how institutional export control policies at clinical sites affect cross-border data transfers in trials, even below DOJ Bulk Data Rule thresholds.