xShare Open Call for Clinical Research
This prestigious recognition honours the vanguard of clinical research innovation, real-world evidence (RWE), and next-generation data strategies. A peer-reviewed validation from European regulators, methodology experts, and CRO leaders — ranking Eclevar first in Europe.
A rigorous, peer-reviewed recognition from a panel of European regulators, methodology experts, data specialists, and CRO leaders.
Prepared for the seamless, secure health data sharing mandated by the European Health Data Space — architected for regulatory interoperability from day one.
Moving beyond experimental phases into ready-to-deploy, high-impact clinical solutions — built for real programmes at scale across the EU.
Built to meet the future of EU clinical research with forward-thinking regulatory architecture that anticipates tomorrow's Notified Body expectations.
For medical device manufacturers, this award validates a partnership model that drastically reduces strategic risk. We have evolved beyond trial execution to become Clinical Evidence Architects.
Every therapeutic area — Cardiovascular, Wound Care, Orthopaedics and Spine — is led by in-house clinicians with direct exposure to Notified Bodies and Expert Panels.
Our proprietary AI-powered platform for intelligent, high-fidelity data collection and real-time monitoring. Built in-house — not outsourced, not off-the-shelf.
Future-proofing PMCF programmes and RWE strategies through interoperable data reuse and regulatory-compliant architecture aligned to EHDS.
Being "just another CRO" is no longer enough to navigate EU MDR and EHDS. Here's why Eclevar is the partner of choice versus traditional generalist CROs.
While traditional CROs rely on generalist Project Managers and CRAs, Eclevar is led by in-house clinicians specialised in Cardiovascular, Wound Care, Orthopaedics and Spine.
Our in-house experts bring recent exposure to Notified Bodies and actively sit on Expert Panels — ensuring your strategy meets the exact scrutiny of European regulators.
Most CROs outsource their data management. We keep our Biometry Department in-house to ensure total data integrity, speed and seamless integration from protocol to database lock.
We don't use third-party tools. We built our own in-house EDC/eCOA and the award-winning MILO platform — purpose-built for EU MDR Annex XIV compliance.
Horizon EU & Investor Backed
Our vision is validated by Horizon EU funding and strong investor support.
Whether you are building a new medical device or a complex RWE strategy, let's discuss how our award-winning data strategy and clinical leadership can secure your market position.
