Event

Regulatory check-up: 1 hour free consultancy

September
14-14
Online

This offer is available every second Tuesday of a month

Since May 2021, the new EU Medical Devices Regulation ((EU) 2017/745 Regulation on medical devices (MDR)) has come into force, and from May 2022, the new EU In-vitro Diagnostics Regulation ((EU) 2017/746 Regulation on in-vitro diagnostic medical devices (IVDR)) will follow it. This will be accompanied by far-reaching changes, including in the classification, clinical testing, and quality management of medical devices and in-vitro diagnostics.

Medidee offers you an exclusive free check of your situation with regard to the new regulatory requirements.

 

Registration:

Medical device and in vitro diagnostic companies can sign up for one of the monthly appointments by using this webpage: Regulatory Check Up – Medidee Services

Media Gallery, Downloads & Info Sheets
Check out our latest newsletter
EIT Health Germany press kit (German only)
EIT Health Germany - facts & figures (German only)