As you noted, we have authorities under the natural health products regulations. These deal with the authorities under Vanessa's Law. Currently, under the natural health products regulations, a company is required to provide adverse reaction reports within 15 days if they are serious domestically, or serious and unexpected internationally. The reporting in Vanessa's Law, which is not in effect yet—you need regulations to bring that into effect—would be mandatory reporting of adverse reactions in hospitals, the way we do for prescription and non-prescription drugs.
If I could use this opportunity, there was one comment made in committee previously about Health Canada already having the authority to make a label change—to add, for example, a serious warning to a label. That is something in Vanessa's Law. It is not in the natural health products regulations. If you take this out of Vanessa's Law, we lose the ability to make a change to a label in order to add a serious warning in the case of a serious or imminent health risk.