I was just going to add, which might bring clarity to your question, that there are two types of approvals in CAMR. There's approval to get on the list, so the idea is that it's a drug that's needed to deal with a health care emergency.
That's not the same as the Health Canada review for health, safety, and efficacy. That's done once somebody manufactures new product X. Health Canada will look at the chemical formulation of those pills and assess whether they're safe and efficacious. That is not the same as the authorization we're talking about in this clause.