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Überprüfungen von Klasse I Herstellern durch Behörden laufen vermehrt an. Was derzeit passiert und was man unbedingt beachten sollte.
Nov 9, 2021
 by 
Daniel Laufersweiler
Medical Device Regulation
Digitalization of QA RA
Aug 16, 2021
 by 
Daniel Laufersweiler
Medical Device Regulation
Interview: Regulatory 4.0
Apr 14, 2021
 by 
Michael M. Kania
Medical Device Regulation
Integrated e-IFU Solution
Oct 26, 2020
 by 
Medical Device Regulation
From OEM to Contract Manufacturer
Sep 26, 2020
 by 
Michael M. Kania
Medical Device Regulation
TÜV Rheinland: EU-MDR & Digitalization
Aug 31, 2020
 by 
Johann Töws
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How to manage Technical Documentation in the most efficient way?
Medical Device Regulation
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Medical Device Regulation
TÜV Rheinland: EU-MDR & Digitalization
Medical Device Regulation
State of the art GSPR
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Fabian Muks
Michael M. Kania
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