Unpredictability of MDR a Major Theme at EU MedTech Forum 2022
Author: Criterion Edge Writers Concerns and frustration surrounding the implementation of Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) were voiced in early May at MedTech Europe’s 2022 […]
[FREE WEBINAR] How to Establish the State of the Art Within the Scientific Validity Report
Click here to watch the recording of this webinar. In this practical presentation, Criterion Edge presents focused strategies on building an IVDR-aligned State of the Art (SOA) section within the […]
[FREE WEBINAR] How to Establish the State of the Art Within the Scientific Validity Report
Click here to watch the recording of this webinar. In this practical presentation, Criterion Edge presents focused strategies on building an IVDR-aligned State of the Art (SOA) section within the […]
