The US Food and Drug Administration (FDA) plans to tackle security issues related to medical devices and has released a plan of action it means to implement in the near future. Broadly, plan is as follows: Establish a robust medical device patient safety net in the US Explore regulatory options to streamline and modernize timely implementation of postmarket mitigations; Spur innovation towards safer medical devices; Advance medical device cybersecurity; and Integrate CDRH’s premarket and postmarket … Continue reading FDA plans to improve medical device cybersecurity