What happens on a licensing decision is that there's the responsibility of Health Canada as the regulator, and the company is the regulatee. So we put conditions on them. What would happen in the case of the patient focus groups is that they would submit their plans for the patient focus groups to Health Canada--how they were going to do patient recruitment, what questions they would ask, where they would be conducting them, what type of structure it would have--and then we would review that and approve or make changes as appropriate.
On November 21st, 2006. See this statement in context.