Milo eCRF is a fully customizable and intuitive Electronic Data Capture (EDC) solution, validated according to ISO 14155:2020 standards. It is designed for medical device manufacturers who want to conduct compliant, efficient, and remotely monitored clinical trials.
From AI-powered patient recruitment to real-time data analytics, Milo Healthcare streamlines every aspect of your clinical trials while ensuring full regulatory compliance.
Easy to manage your data
Collaborate securely
Accelerate your clinical research
Finalization of the eCRF
Faster Cleaned Data
Simplified Export of CERs
Collect scientifically valid PMCF data that complies with the MDR using our platform
Easily comply with GDPR requirements for informed consent and data protection.
Our in-house data protection officer monitors compliance for all studies.
Our platform meets the requirements of ISO14155:2020 and GDPR.
All data entries automatically include user identification to ensure fully documented traceability from source to sponsor using advanced AI technology.
Conducting clinical trials can be overwhelming due to documentation and compliance tasks—but with Milo, everything has become easier, faster, and more manageable.
Dr. Axel Schulz
Orthopedic and Trauma Surgeon
OSSUR
Highly innovative and powerful for our trial on diabetic foot ulcers.
Antoine Turzi
CEO
RegenLab
We tested Milo in a clinical trial, and it was extraordinary and promising for advancing research.
Prof. Luc Teot
Director of Cicat-Occitanie
CHU Montpellier
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