TÜV SÜD Danmark ApS receives designation as Notified Body in accordance with MDR 2017/745
TÜV SÜD Danmark ApS today received its designation as Notified Body 2443 under Medical Device Regulation 2017/745 by the…
TÜV SÜD Danmark ApS today received its designation as Notified Body 2443 under Medical Device Regulation 2017/745 by the…
TÜV SÜD is one of the few notified bodies that still has capacities for conformity assessment procedures for medical dev…
The Notified Body TÜV SÜD Product Service GmbH released the first certificate for a non-medical purpose device according…
The established online event TÜV SÜD Digital Dialogues, which brings together global experts and industry thought leader…
TÜV SÜD is calling for further advancement of the procedure used for mandatory penetration testing for medical devices a…
Integrated approaches to the testing of medical lamps are becoming increasingly necessary in the face of factors includi…
SoundTrack_Cologne presents four high profile case studies in which music plays a significant and exemplary role – and i…
On 6 January 2023, the European Commission published a proposal to amend the Medical Device Regulation (MDR) and the In…
TÜV SÜD Digital Dialogues is an established online event that brings together global experts and industry thought leader…
TÜV SÜD Digital Dialogues, the digital format developed spontaneously by the testing and certification provider in respo…