The Federal Drug Administration published new requirements mandating security standards for newly submitted medical devices. Samantha Jacques, vp of clinical engineering, McLaren Health, doesn’t see this impacting large manufacturers as much, given they already make these devices compliant with more stringent European standards. Rather medium and small-sized manufacturers will need to play catch up to get new devices to market.
Got feedback? Join the conversation on LinkedIn.
Huge thanks to our sponsor, Claroty
