That's the magic. Nobody knows which ones you're going to follow up on. It's all good. We all have to behave.
Madam Yeates, I want to focus on the transparency issue. You've heard the passion on all sides of this committee. As parliamentarians we understand the importance of sharing information with the public. When it comes to authorized drug trials, there are a few aspects that I want your view on.
It's important for those in the trials to have access to the information. This is also important for people who end up on those drugs. I would suggest it's very important for Canadians who are making a decision about taking that drug. We are now seeing more and more that people's physicians will say to take a drug, and people will say, wait a second, and they're going to the Internet and they're verifying it. Certainly, parents do that for their children all the time. Obviously, the Auditor General focused in on your risk-based approach with regard to the inspection of clinical trials. There were a number of cases of non-compliance that you had also determined.
What actions are you taking, as a department, to disclose the information related to the clinical trial inspections in those three parts: the participants, the prospective users, and the users?