Atlantia Clinical Trials

You've looked at Atlantia. Here's the actual detail: full visibility into your budget, recruitment and timelines, 40,000+ participants in our recruitment database, and a team that runs your trial end to end. Watch the two-minute breakdown.

Wearables and self-monitoring are shifting care into the home, putting medical devices at the centre of it. Our CCO explains how Atlantia runs the trials behind that shift: full-service design, organisation and execution, in-house recruitment from 40,000+ participants, and full visibility into budgets, recruitment and timelines throughout. We specialise in Class 2 devices, reporting to the FDA and equivalent European bodies.

Medical device research spans a lot of ground — first-in-human studies, wearables, remote monitoring, and IVD. Most CROs are set up for one or two of these. Fewer are built to run all of them well. Atlantia works across the full range, from early feasibility through to post-market studies, with our own clinics in Cork and Chicago. If your programme touches more than one of these areas, it helps to work with a CRO that already does. See what we cover.

For complex devices, Notified Body reviews take 13 to 18 months, and fees for Class III have exceeded €165,000 before adding in audits or PMCF. Budgets built on MDD-era assumptions won't cover it. We’ve compiled a guide on the real cost of MDR and IVDR compliance, including post-market activities that are rarely factored into the pre-market budgets. You can use a checklist to go over your own numbers. Atlantia has supported MDR, IVDR and CE-marking submissions for over 200 studies, run from our own clinics in Cork and Chicago.

Device trial budgets rarely survive initial contact with the real study. 30–40% of sites under-enrol. More than 3 in 4 run late. And budgets per patient can range from €12,000 to €43,000, depending on the device. Get a guide that addresses device trial budgets: The money that commonly gets overlooked, sizing your trial at exactly what regulators want, and what to look for in a CRO's bid before you sign. Download for free. The guide comes with a checklist for budgeting the trial ahead. Built on Atlantia's experience across 200+ device studies, run from our own clinics in Chicago and Cork. Free to download.

Looking for a CRO that can manage specialised clinical investigations from start to finish, while keeping timelines and budgets under control? Atlantia provides scientific and operational expertise across clinical and regulatory requirements, with flexible solutions to suit a range of budgets. By working outside large hospital networks, we help reduce overhead, minimise protocol deviations and support efficient participant recruitment. This allows studies to move faster and helps ensure your funding is spent where it matters most. Discover how Atlantia can help reduce clinical study costs, speed up timelines and deliver clear study findings.