Logo Eclevar

The Ideal Post-Market Survey solution for MedTech

Collect scientifically valid and compliant post-market data using Patient level Survey Solutions, specifically built for medical device and diagnostics post-market surveys under EU MDR and FDA. 

Tailored Solutions
Easy-to-use app
Bring your own device
Patient compliance
Robust training
Therapeutic alignment
Trigger Downstream process

Milo allows sponsors to create diaries

Milo Builder accommodates robust reporting and integration. It’s dynamic and fully customizable and can be modeled on multiple devices in real time.

Protocol changes can be made centrally to patient assessments and deployed automatically to all participants. This helps you reduce risk and study delays. 

Participants use the Milo App to add diary entries

Milo Patient increases compliance and enhances the patient experience. It’s intuitively designed for Android or iOS using consistent features available online or off. 

Whether with a provisioned device or bring your own device (BYOD), Scribe updates studies without requiring patients to download an updated app.

Interface ePRO and eCRF

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Milo patient survey Mobile

Milo DCT makes it easier to capture your trial data and integrate it seamlessly with other data in your clinical trial ecosystem.

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The Site Qualification collaborated with Companies, investigator sites, CROs to achieve the goal of enhancing and simplifying clinical trial

MILO Survey Analytics

Milo Site Contracts solution combine clinical trial contract best practices, local knowledge and know-how, and proprietary automate process tools

Custom eCOA library reduces Clinical trial Orthopedic and spine program timelines by 50%

Level 4 high-quality surveys are patient-reported outcomes questionnaires and are intended to measure a patient’s health-related status or quality of life at a single point in time. In addition,  level 4 high-quality surveys are self-completed questionnaires and are collected over a short period of time. PROM level 4 information is collected before and after a procedure/surgery and provides an indication of the outcomes or quality of care delivered to patients. 

Discover how a large spine sponsor created a customized eCOA library to collect accurate, daily-reported patient data across 13 countries. There was no room for error; each input needed to roll up into one resolution.

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Case study of the MILO platform

How Regenlab and Unither Pharma Mastered Mid-Study Changes with MILO's Seamless ePRO Integration

MILO’s ePRO solution enabled Regenlab and Unither Pharma to engage with a participant population that might otherwise struggle with a technology solution they had never used before.

Easy-to-use ePRO surveys, accessible to participants on familiar devices, made real-world data collection possible. Native integration with MILO allowed Regenlab and Unither Pharma to collect and manage data seamlessly, conserving budget and IT resources that would typically be spent sourcing and integrating with additional vendors. 

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ePRO questionnaire

Native ePRO questionnaire created within Milo EDC

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Send invitation

Send email (QR code to download app) or login to mobile site

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Responsive Survey

Participants fill out the survey on a laptop or mobile device

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Notifications

Receive app/email notifications reminding when to take the survey

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ePRO Data Capture

ePRO data captured in Milo EDC

Get Started with Milo Today

Transform your site contracting process with Milo’s advanced platform. Contact us today to learn more about how Milo can help you streamline your clinical trials and achieve faster, more efficient results

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Weeks Study Start-up

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LEADERSHIP TEAM

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Obuchinezia Anyanwu

Head of
eCOA/ePRO
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Romain de Montalivet

Team leader
Clinical Operations
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Dr. Nikhil Khadabadi

Chief Medical Officer, Orthopedics and Spine
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Guillaume CHARLES

Study start-up and Site partnership
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Anna Hodge

Senior
Biostatistician

Recent Publications

At Eclevar, we pride ourselves on providing comprehensive and innovative solutions to enhance clinical trial management. Our clinical team have recently published several studies focusing on Survey Levels in clinical trials, highlighting the critical role of surveys in collecting real-world data and optimizing trial outcomes. 

Wearable Technologies for Children with Chronic Illnesses: An Exploratory Approach.

McErlane F, Davies EH, Ollivier C, Mayhew A, Anyanwu O, Harbottle V, Donald A.Ther Innov Regul Sci. 2021 Jul;55(4):799-806. doi: 10.1007/s43441-021-00278-9. Epub 2021 Apr 12.PMID: 33844190

An algorithmic approach to shoulder pathology.

McErlane F, Davies EH, Ollivier C, Mayhew A, Anyanwu O, Harbottle V, Donald A.Ther Innov Regul Sci. 2021 Jul;55(4):799-806. doi: 10.1007/s43441-021-00278-9. Epub 2021 Apr 12.PMID: 33844190

Demonstrating the feasibility of digital health to support pediatric patients in South Africa.

Davies EH, Fieggen K, Wilmshurst J, Anyanwu O, Burman RJ, Komarzynski S.Epilepsia Open. 2021 Dec;6(4):653-662. doi: 10.1002/epi4.12527. Epub 2021 Sep 2.PMID: 34310860 Free PMC article.

Rewatch Our Webinar: Leveraging Level 4 High-Quality Surveys to Address Clinical Data Gaps

Rewatch Our Webinar: The Three E's - eCRF, eConsent, and ePRO

Get your copy of our new whitepaper today!