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Is the FDA Going Backwards on Devices?
I've always thought that the pharma side was always a lot easier to work with. I feel like more transparent for a long time, they came up with accelerated approval paths for life-threatening diseases. And so it always sort of felt, it was always weird to me doing both biotech and devices. That devices for a longtime was very different, right? And it was just harder to get good feedback that was transparent.