For sure. It speaks to her third point here:
Establish a Canadian Plan for Rare Disorders that is based on international best practices....
That speaks to the network you build to share that expertise. And whether it's Health Canada centred, as in other areas, for instance, a committee for orphan products or rare disorders, or whether you're building it through our institutes or health research, it's a way to coordinate it.
It is federal-provincial, but from the regulatory point it's federal leadership. The provinces need to know we're all talking about the same thing. Today, across the country everyone is defining it differently, and it is creating a lot of confusion. That's where part of the problem comes in as well.