Start Your Clinical or Regulatory Journey with Confidence
Partner with Europe’s leading MedTech and IVD CRO to fast-track compliance, accelerate approvals, and bring your innovations to market.
Request Your Free Expert Consultation
Get a no-obligation, expert-led consultation to discuss your clinical or regulatory needs. Just share a few details, and a senior consultant from our IVD or Medical Device team will be in touch within 48 hours.
Why Partner with MDx CRO ?
MDx is your trusted full-service CRO specializing in Medical Devices, IVDs, Software as a Medical Device (SaMD), and Companion Diagnostics.
Our tailored solutions cover everything from regulatory consulting and clinical research to quality assurance and usability engineering, all aligned with MDR and IVDR requirements.
Whether you’re launching a Class III medical device, conducting a CDx trial, or transitioning from IVDD to IVDR, our expert team is here to support your journey—strategically, globally, and compliantly.
Our Locations
Barcelona
Lisbon
London
Madrid
Your CRO Partner for Global Success
Looking for a European CRO partner that’s agile, knowledgeable, and fully equipped to guide your clinical and regulatory journey?
Whether you’re launching a Class III medical device, preparing a CDx trial, or transitioning from IVDD to IVDR, MDx CRO is here to accelerate your path to market with full-service support.
