I'll speak to both of those questions.
In terms of the adverse event reporting, first of all, currently no one submits that information to us, and there are no plans for that at the current time. We certainly believe that efficiency in data information is our strength. We think we're very good at standardizing databases. We have good relationships with data providers and in general we think we're a very good place to standardize data. Just as we are able to do that, develop NPDUIS, and then we have agreements with the submitting jurisdictions that we can give access to that data to PMPRB with their regulatory mandate, it's certainly possible that we could, if it were desired by all involved, perform that function as well.
I do think there is some efficiency to be gained by having the data collected as few times as possible, rather than in numerous ways.