Mr. Chair, in response to the member's question, first and foremost, there is specific information on all of the drugs we've approved, and through MedEffect and CARN, any adverse events that are being reported to us.
While we acknowledge that people take individual drugs, we provide information on that individual drug and the types of adverse events, updates, and warnings to both health professionals and to the general public. That information is, and will continue to be, made available.
On clinical trials, we're looking to expand it, as well, in the early stages of the product development.
With respect to user fees, we are at this point posting aggregate information, but we could, obviously, provide detailed information.
I would have to pause on my answer there and just confirm exactly what level of detail our accounting system and others would be able to put forward, but we can commit to transparency on both the fees we're collecting and the performance standards we're using to meet those.