eCRF Platform Hero - Dark Elite

eCRF Platform

The #1 All-in-One Solution for Your Next Clinical Trials

eCRF (Electronic Case Report Forms) — Build, Recruit, and Monitor Your Study from a Single Platform. Connect Clinicians, Hospitals, Industry Professionals, CROs, and Patients.

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Next-Generation EDC

Milo eCRF - The Next-Generation EDC Platform for Medical Devices

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.

eCRF Features & Benefits - Dark Elite

Key Features

Turn your data into proactive decisions

Access to fully customizable dashboards
View important data (patients, sites, forms)
AI-driven insights with user-defined rules
Anticipate risks before they arise

Create eCRFs and surveys in seconds

Intuitive drag-and-drop builder
No coding required
Creation of PROs, safety reports, clinical criteria
Simple and compliant deployment

Monitor recruitment & study progress in real time

Tracking patient visits, screening failures, inclusion milestones
Dynamic dashboards updated automatically
Instant alerts for queries or delays
Complete control over site performance and schedules

Transform your medical device research with our comprehensive EDC solution

From AI-powered patient recruitment to real-time data analytics, Milo Healthcare streamlines every aspect of your clinical trials while ensuring full regulatory compliance.

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Easy to manage your data

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Collaborate securely

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Accelerate your clinical research

eCRF Platform Stats & Testimonials - Dark Elite

Milo eCRF Performance

100%

Finalization of the eCRF

50%+

Faster Cleaned Data

100%

Simplified Export of CERs

Benefits of Using an Electronic Data Capture System in Clinical Trials

Collect scientifically valid PMCF data that complies with the MDR using our platform.

GDPR compliance made easy

Easily comply with GDPR requirements for informed consent and data protection.

Our in-house data protection officer monitors compliance for all studies.

Pre-validated & compliant data platform

Our platform meets the requirements of ISO 14155:2020 and GDPR.

Fully documented data traceability

All data entries automatically include user identification to ensure fully documented traceability from source to sponsor using advanced AI technology.

ECLEVAR

MILO eCRF

Unmatched expertise to conduct your trials with assured quality and provide patients with safe and innovative therapies

What Our Clients Say

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