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Medical Devices

 

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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About Avania

Avania is an integrated global, full-service CRO with specialized expertise in medical device, novel technology, and combination products. They advance products from feasibility all the way through post-approval trials in analytics, clinical trials, consulting, regulatory, reimbursement, and more.

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      • Clinical Safety Management
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    • Reimbursement
  • Solutions
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      • Aesthetics
      • Cardiovascular
      • Dermatology
      • Neurology
      • Ophthalmology
      • Orthopedics
      • Urology
    • Industry Expertise
      • Medical Device
      • Medical Technology
      • In Vitro Diagnostics
      • Biotech
    • Specialized Expertise
      • FIH and EFS
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