Hi All
Due to recent European legislation about protecting medical devices, European Union regulators put forward a new set of market entry requirements for medical devices and in vitro diagnostic medical devices to reduce the risk of patient harm as a result of a cyber incident, as well as protect national health systems.
https://www.darkreading.com/edge-articles/how-europe-is-using-regulations-to-harden-medical-devices-...
Regards
Caute_Cautim
