When You Need to Advance Your Final Medical Device to the EU Market, It Takes Avania.

Avania’s specialized expertise in medical device, novel technology, and combination products supports your product from feasibility all the way through post-approval trials in analytics, clinical trials, consulting, regulatory, reimbursement, and more. Watch our webinar to learn more about the key requirements with respect to clinical evidence in the EU, how to identify key milestones in clinical development, as well as what can be considered a relevant source of clinical evidence in the premarket phase.

View the Webinar

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