Looking at the actual sections of this division, I want to zero in on the test. It says:
Subject to any regulations made under paragraph 30(1)(j.1) and if the Minister believes that the use of a therapeutic product, other than the intended use, may present a risk of injury to health, the Minister may....
Then, of course, it establishes rules on the conditions.
I'm wondering how you feel about the subjective belief test. Do you think that's an appropriate measure to apply to potentially removing products from consumers, or should there be some objective standard imported into that section?