Recently we took part in a webinar with Health-ISAC which is now available ON DEMAND!
Medical Device Cybersecurity: A Holistic Approach to Decrease Attack Surface & Improve Patient Safety
Featuring panellists: Tyler Gannon, Phil Englert, Larry Pesce, Justin Heyl
There have been many articles written about the Internet of Things in the last 12 months, and these have created a considerable amount of confusion in the marketplace. What is clear, however, is that the computing industry is shifting to a new model, even if it doesn’t quite understand what it is.
Back in May 2017 the EU, through its Medical Device Coordination Group (MDCG) published the Medical Device Regulation (MDR) (EU) 2017/745, which came into effect on 25th May 2017. The regulation was put together to ensure high standards of quality and safety for medical devices being produced in or supplied into the EU. Manufacturers of currently approved medical devices have until May 26th, 2021 to meet the requirements of the regulations. Even if a product is Medical Devices Directive (MDD) compliant, they still need to meet these new regulations.
