Medical Devices

White Paper

China: NMPA and the New Medical Device Regulations

Webinar

Collecting Clinical Evidence In The Post-Market Era

Webinar

Collecting and Evaluating Clinical Evidence In The Pre-Market Phase

Fact Sheet

Medical Writing Fact Sheet

Fact Sheet

Analytics Fact Sheet

Blog

EU Medical Device Regulation 2017/745 – First Formal Amendment, Delaying Date of Application

May 4, 2020

Blog

Post-market surveillance under a “522 order” — why, what, and how?

April 9, 2020

Blog

Medical apps under the new European MDR

April 6, 2020

Blog

What Can Your Reimbursement Support Services Team Do for You?

April 6, 2020

Blog

Clinical Evaluation Plan – The Start of All Clinical Evaluations

April 6, 2020

Your product is important, and your trial deserves the team that has what it takes. It takes knowledge. It takes passion. It takes commitment. It Takes Avania.

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