Another question that I've asked of previous panels is on the regulation of medical devices, which is solely a federal jurisdiction.
We’ve heard complaints that it's difficult. We also heard one doctor who said it was much easier than his attempts in the U.S., that it was quite easy to deal in Canada.
For any of the panellists, what are your impressions on the regulation of medical devices, given that they are tools of innovation? Are we making a system that is supportive of enabling that type of innovation?