No, no, I appreciate that.
There's a question I want to pose to both Jacquie and Allan. It's a question I've asked panels before. We've had a series of panels on technological innovation.
When it comes to areas that are strictly in the federal jurisdiction—a lot of health care, obviously, is provincially administered—one area that is a tool for innovation is the regulation of medical devices. One doctor who came in here said it was a slow process, and another said it was excellent compared with the U.S., where he had dealt with this.
What are your perspectives on the regulation of medical devices with any of the organizations or groups that you've worked with? Are there improvements that can be made in Canada, or do we have the right balance right now?