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Regulatory Consultant

CHICAGO, United States

https://www.clinicalevaluation-report.com

We're here to advise and support you on a wide range of regulatory documentation and cGMP advisory solutions..

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FDA Wants to Increase Diversity in Clinical Trials

April 21, 2022

EU provides guidelines for high-risk IVDs as well as surveillance of older medical devices

March 1, 2022

Device group calls on FDA to further refine it’s the guidance on software functions

February 24, 2022

A medical device company practical guide to the PMCF requirements of the EU MDR

January 25, 2022

CE Marking Consultants and EU Quality Management System Certificate

November 16, 2021

Top 20 Medical Device Acronyms & Terminologies You Must Know

September 29, 2021