Thank you very much for the question. I am Celia Lourenco, with the health products and food branch of Health Canada.
We're aiming to introduce three new authorities at the level of the act, starting with what we call the “supplementary rules of authority”, which will allow us to have a ministerial order put in place to address situations in which products are being intentionally misused. An example would be the nicotine replacement therapies—the nicotine pouches—that are being used by youth. We want to be able to put in place rules around place of sale and around labelling, packaging, flavours and other aspects that would be appealing to youth. That's one objective.
That particular authority does not at all intend to limit or restrict off-label users or the use of health products in the context of the health care system. It's really for situations in which there's intentional misuse or diversion of a product for use completely outside of health.
The second rule is around exemption: being able to exempt products from the Food and Drugs Act and regulations. A particular example there is that over the last two years we've unfortunately had a shortage of infant formula. Currently, we don't have in our framework the ability to exempt foreign products and foreign formulas that are nutritious but may not completely meet our regulatory requirements around labelling, for example.
We want to be able to bring in those products in order to meet that unmet need but to do that quickly through a ministerial order that would have rules in place around those products.