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Join us in transforming medical device clinical research with innovative AI-powered solutions and a proven track record of excellence

Eclevar is a CRO created in 2018 and based in Paris La Défense. We work across the entire value chain of medical device development, through complementary services tailored to our clients' challenges. We offer customized service, personalized to the need of our clients. Whether you are looking for full service CRO or staffing clinical or regulatory experts, our management team with more than 20 years experience will drive you to the effective solution.

A Company Shaped by Innovative Minds

Eclevar is a team of passionate experts with strong skills and experience in their field of expertise. Our team is composed of multilingual professionals who have worked in the medical device, pharmaceutical, CRO and notified body industries.

We combine deep regulatory expertise with cutting-edge technology to deliver exceptional results for our clients across Europe, Asia, and beyond.

Key Metrics & Achievements

40+
Team Members
43+
MedTech Companies Supported
20+
Languages Supported
95%
Revenue from Medical Devices
12 mo
Average Client Retention
€200K
Average Trial Cost

Why Invest in Eclevar MedTech?

Proprietary Technology Platform

MILO Healthcare is our AI-powered, all-in-one EDC platform for medical device trials, featuring eCRF, ePRO, eConsent, Survey, Cohorts, and Randomization modules. Fully compliant with 21 CFR Part 11, ICH-GCP, GDPR, HIPAA, HL7 FHIR, OMOP CDM, and DICOM.

Proven Market Demand

With the EU MDR creating unprecedented demand for clinical evidence, we're positioned at the intersection of regulatory compliance and technological innovation. Our clients span cardiovascular, orthopedic, wound care, and other high-growth therapeutic areas.

Experienced Leadership Team

Our management team brings over 20 years of combined experience in medical devices, clinical research, and regulatory affairs. Led by CEO Chems Hachani and supported by world-class advisors including Prof. Luc Teot and Dr. Nikhil Khadabadi.

Global Reach, Local Expertise

Operating across France, UK, Germany, Japan, and Australia, we offer localized expertise with global standards. Our multilingual team navigates complex regulatory landscapes including EU MDR, PMDA, TGA, and FDA requirements.

Scalable Business Model

Our dual revenue streams—CRO services and MILO Healthcare platform subscriptions—create a scalable, recurring revenue model. Platform pricing ranges from €500/month to €3,000/month for unlimited studies.

Strong Client Retention

With an average client relationship of 12 months and testimonials from industry leaders like Ossur, RegenLab, Pfizer, and CHU Montpellier, we've built lasting partnerships based on exceptional service delivery.

Market Opportunity

Growing Regulatory Demand

  • EU MDR implementation driving unprecedented demand for clinical evidence
  • Stricter post-market surveillance requirements (PMCF)
  • Increased scrutiny from notified bodies
  • Global harmonization creating opportunities across multiple markets
  • Rising complexity requiring specialized CRO expertise

Technology Disruption

  • AI-driven patient recruitment reducing trial timelines
  • Real-time data capture improving data quality
  • Automated transcription (MILO Voice) streamlining workflows
  • Cloud-based EDC platforms enabling remote monitoring
  • Integration with EMR systems reducing manual data entry

Competitive Advantages

  • Proprietary MILO Healthcare platform differentiates from traditional CROs
  • Deep expertise in medical device regulations (EU MDR, ISO 14155)
  • Strong network of investigators and clinical sites
  • Multilingual capabilities across 20+ languages
  • Recognized by BSI as MedTech experts in PMCF Guide

Growth Strategy

  • Aggressive SEO and digital marketing campaigns
  • Strategic partnerships with healthcare institutions
  • Expansion into new therapeutic areas (cardiovascular, pediatric)
  • Platform subscription model for recurring revenue
  • Geographic expansion in Asia-Pacific and North America

Ready to Invest in the Future of MedTech?

Join us in transforming medical device clinical research and making a real impact on healthcare outcomes worldwide

Schedule a Meeting with Our Leadership

Get your copy of our new whitepaper today!

investors,CRO,investment,start-up healthcare,become investor,contact us,innovative,investor