Medical Devices

White Paper

Beyond the CE Mark: How to Collect Clinical Evidence to Ensure EU MDR Compliance

White Paper

Navigating the Pre-Market EU MDR Journey

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

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