With respect to the first part of that question, I can say that from a compliance and enforcement standpoint, when we look at issues, including labelling issues, what we find is that lots of companies are in non-compliance, or in contravention, with their market authorization. As the member says, it is something that's not allowed under our legislation, nor would their market authorization allow them to make a claim, but in some cases, you still find the claim. Then, they are in direct contravention with the Food and Drugs Act and the regulations, and that is where our compliance enforcement would come in, including such tools as stopping sales, seizing product, and public communications. That would be in contravention of a market authorization, the act and the regulations.
Deputy, I think I will ask Pam if she would like to add anything.