From our perspective, regulatory data is one thing. Regulatory data is what's required for your submission, and it's outlined very prescriptively by the PMRA in terms of which data are required to satisfy which elements of the review. Those are the data that our members provide as part of the registration. Any other studies—public studies, academia studies—that the PMRA looks at as part of, for example, a re-evaluation, are all looked at as part of their package.
Now, how they reference those in the final document is, I think, what you're getting at.