A general question I've asked each panel so far that we've had on health technological innovation has been about the federal role in the regulation of medical devices and products, because that's another area where there's federal jurisdiction.
Have any of you been involved in a medical device or a product, and what has been your experience? What impressions do you have about how we could become more efficient on medical devices? Is there a lot of red tape in that process? Do you believe we have an atmosphere or an environment that fosters and enhances innovation, or is government a roadblock in that?