Cybersecurity for Medical Devices in the UK: Protecting Lives in a Digital Age
August 17, 2023
Cybersecurity for Medical Devices in the UK
Showing 36 to 40 of 101
August 17, 2023
Cybersecurity for Medical Devices in the UK
August 15, 2023
The appointment of an EU Authorized Representative (EU AR) is a significant challenge for manufacturers outside the European Union (EU) seeking to enter the EU market.
August 10, 2023
RQMIS is an EU Authorized Representative. What does that mean for you?
August 8, 2023
Software as a Medical Device (SaMD) has transformed healthcare, but complying with the intricate regulations in the EU and UK can be challenging.
August 3, 2023
The revised guidance includes requirements for how FDA provides feedback through the Q-Sub process in line with goals outlined in MDUFA V.