FDA requirements were the first thing that popped into my mind. Is it possible somehow these devices fall under different regulations than “medical devices”? I am only vaguely familiar with the applicable 21 CFR regs. This seems like a pretty gargantuan screw up since it could, I would think, kill people.
FDA requirements were the first thing that popped into my mind. Is it possible somehow these devices fall under different regulations than “medical devices”? I am only vaguely familiar with the applicable 21 CFR regs. This seems like a pretty gargantuan screw up since it could, I would think, kill people.
It’s class III medical device software