Contact โ€” Eclevar Medtech
Contact Eclevar Medtech

Let's architect your
clinical success.

Our global regulatory and clinical experts are ready to de-risk your device program. Connect through our direct channels or visit our global hubs.

48h Max Response
4 Global Hubs
EU MDR Specialists
Strategic Inquiries
clientcare@eclevar.com

Request a tactical roadmap or book a CER strategy session.

Global HQ Line
+33 01 87 66 24 12

Paris HQ โ€” Central European Time (9:00โ€“18:00).

Talent & Careers
careers@eclevar.com

Join our team of former NB reviewers and clinical architects.

Get in touch

Tell us about
your program.

Whether you're navigating your first EU MDR submission or scaling a global clinical investigation, our senior strategists respond within 48 hours.

Direct access to senior regulatory experts
EU MDR 2017/745 ยท ISO 14155 ยท PMDA specialists
All inquiries handled with strict confidentiality
GDPR compliant โ€” your data stays in the EU
Direct channels

Three ways to start.

01

Strategy Call

Book a 30-min discovery call with our clinical leads. We map your regulatory path in a single session.

Schedule Now
02

Technical File Audit

Get a quote for a reviewer-grade Gap Analysis. Our former NB auditors know exactly what examiners look for.

Request Quote
03

MILO Demo

Experience our proprietary clinical data and cost modelling platform, live with your own trial parameters.

View Platform
Global Command Centers

A connected
infrastructure.

Four strategic hubs covering every major regulatory corridor.

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Paris

10 Rue de la Paix,
75002 Paris, France

EU Regulatory HQ
๐Ÿ‡ฌ๐Ÿ‡ง

London

128 City Road,
London, EC1V 2NX, UK

UKCA Corridor
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Tokyo

Shinjuku Park Tower,
Nishishinjuku, Tokyo, Japan

PMDA Expertise
๐Ÿ‡ฎ๐Ÿ‡ณ

Pune

World Trade Center,
Kharadi, Pune, India

MILO Tech Hub

Recognized Excellence in Medtech CRO Services

Eclevar Medtech Awards 2026
EU MDR 2017/745 ISO 14155:2020 ISO 13485 21 CFR Part 11 GDPR Compliant

Reforming Clinical Evaluation of Medical Devices in Europe