Certainly, getting this done on a regular basis, informally at this point, I think we rely on a lot of the information from the FDA, for example. I think there's unquestionably a possibility of working together with the other groups, such as the FDA, to consolidate the information. Many of these trials, of course, are done internationally in any event, so I don't think it would be a problem.
Evidence of meeting #51 for Health in the 39th Parliament, 1st session. (The original version is on Parliament’s site, as are the minutes.) The winning word was cdr.
A recording is available from Parliament.