From orthopedics to cardiovascular, wound care to aesthetics — Eclevar delivers specialized clinical trial expertise across every therapeutic area.
At Eclevar MedTech, we understand that every therapeutic area has unique regulatory, clinical, and patient-centered requirements. Our multidisciplinary team brings deep expertise across all medical device categories, ensuring your clinical trials are designed, executed, and reported to the highest standards — no matter the indication.
Joint replacements, spinal implants, trauma devices, and bone regeneration solutions.
Learn More →Advanced dressings, negative pressure therapy, skin substitutes, and chronic wound management.
Learn More →Stents, heart valves, pacemakers, defibrillators, and vascular access devices.
Dermal fillers, laser devices, skin rejuvenation, and cosmetic implants.
Intraocular lenses, glaucoma devices, retinal implants, and vision correction systems.
Dental implants, bone grafts, orthodontic devices, and maxillofacial reconstruction.
Neurostimulators, cranial implants, shunts, and brain monitoring devices.
Urinary catheters, pelvic floor devices, contraceptive implants, and fertility solutions.
Surgical staplers, mesh implants, laparoscopic instruments, and suture devices.
Ventilators, airway management, oxygen therapy, and respiratory monitoring.
Insulin pumps, continuous glucose monitors, injection devices, and metabolic implants.
Neonatal devices, growth monitoring, pediatric implants, and child-specific solutions.
Our experts have hands-on experience in your specific therapeutic area, ensuring protocols are clinically sound and regulatory-compliant.
We stay ahead of evolving MDR, IVDR, and FDA requirements, tailoring strategies to your device class and indication.
Access to top-tier investigators and clinical sites across Europe, ensuring rapid enrollment and high-quality data.
From protocol design to final report, we manage every aspect of your clinical trial with precision and transparency.
Post-market surveillance tailored to your therapeutic area, delivering robust evidence for CER updates and notified body reviews.
Our proprietary EDC/eCOA platform streamlines data collection, patient engagement, and real-time monitoring across all therapeutic areas.
Clinical Trials Conducted
Therapeutic Areas Covered
MedTech Companies Supported
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Let's discuss how Eclevar's therapeutic expertise can accelerate your path to CE marking and regulatory approval.
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