Medical device clinical trials require highly specialized knowledge and a customized approach. Avania has experience across all medical device classifications. Our team has more than 30 years of experience managing successful medical device clinical trials across more than 30 countries.  

Although we are a medical device contract research organization (CRO) with a global footprint, our personalized approach simplifies the advancement of medical devices for each one of our sponsors. We utilize our collective technical and therapeutic knowledge related to regulatory requirements for study approval, applicable study design options, required safety reporting, and key endpoint data needed to successfully complete a trial.

When you trust your trial to our team, you get a depth of experience and expertise you cannot find anywhere else. Leveraging our expert and flexible team, we successfully deliver your project on time and on budget. All of this makes us the one-stop shop you can count on to take your product from concept all the way through commercialization.

900 + Medical Device & Diagnostic Projects

400 + Medical Device & Diagnostic Clinical Trials

350 + Regulatory

30 + Breakthrough Designations

Your product is important, and it takes a team with medical device expertise to move it forward. It Takes Avania.

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