Common Specifications for Annex XVI products (without an intended medical purpose) now published in the Official Journal of the European Union December 7, 2022
UK MedTech Regulatory Status: ABHI’s Regulatory Conference and Membership Survey raise red flags October 17, 2022
Evnia summarizes the findings of MedtTech Europe’s latest survey report on the implementation of MDR July 20, 2022
Evnia’s latest article on Preference Testing for Medical Devices is now indexed on PubMed! July 18, 2022
Evnia announces the successful completion of ISO 9001:2015 audit for its Authorized Representative, Clinical and Regulatory Affairs Consulting services July 13, 2022
Evnia Group launches Evnia-AR, its new operational branch, to offer Authorised Representative (EC REP) services under MDR/IVDR July 5, 2022
