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Optimize Research with Clinical Trial Database Software

Optimizing eSource Clinical Trials for Efficiency

EDC Database Solutions for Efficient Data Management

Ready to get started building the right eClinical solution for your trial?

87% HIGHER DATA QUALITY

90% PATIENT COMPLIANCE

66% TIME SAVINGS

Revolutionizing research with a single, game-changing, and user-friendly platform!

Integrated solutions encompassing EDC, eCOA/ePRO, eCRF, and eConsent for non-interventional studies, Real-World Evidence (RWE), and successful launches. Enhance communication with healthcare professionals by providing real-time clinical data insights into study progression.

Data Management with eCOA

Milo ePRO automatically provides the necessary audit trail traceability for compliance with clinical trial regulations. Mandatory fields, edit checks, input-dependent paths, and automated validations further enhance the quality of data, ensuring accuracy and reliability.

Extended data analysis

Streamline your study phases and save precious time with Milo's data analysis and visualization capabilities. Stored and pre-filtered views facilitate smoother transitions to subsequent clinical trials, accelerating future setups.

Amplified Patient Input with ePRO

Direct feedback from patients is facilitated by ePRO, streamlining their participation in clinical trials. For instance, the reduced need for on-site appointments allows patients to effortlessly incorporate the upkeep of the electronic patient diary (eDiary, ePRO) into their daily routines.

Each trial is unique. Discover how Milo can assist you.

1

Streamline your process with standardized workflows

Optimize your study kick-off with reusable study, workflow, and notification templates, all on a unified, cloud-based platform for seamless collaboration. 

2

Get on board effortlessly with Total Consent Management

Speed up recruitment and onboarding using digital screening surveys and consent processes. Enhance global trial accessibility, boost participant retention, and reduce compliance errors with Total Consent. 

3

Maximize participant involvement and retention in trials

Ensure trial participant engagement with offline accessibility, cross-platform TeleVisit scheduling featuring waiting rooms, reminders, notifications, and in-app help and support.

4

Elevate your data collection standards with Patient-First Data Generation

Cut down on data cleaning time and focus on swift, meaningful analysis. Unleash the potential of eCOA, Bring Your Own Device (BYOD), and integrated sensors in one powerful solution.

5

Gain comprehensive control over your study

Gain immediate insights into data and participant progress using operational dashboards. Proactively prevent dropouts, identify trends early, and make well-informed decisions in real-time.

TIME & COST SAVINGS

QUALITY AND QUANTITY

DEVICE-INDEPENDENT USE

Milo Goes Global with Distributed Computing Technology (DCT)

USA
BRAZIL
EUROPE
ASIA
Japan

Ensuring Regulatory Excellence: A Commitment to Safety Compliance

Trust MILO for a compliant, forward-looking solution that prioritizes both innovation and safety

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