Ms. Elliott, if we can't rely on the industry, which never did the studies it was supposed to carry out when the moratorium was conditionally lifted in 2006, and we can't count on the surgeons, because it's impossible to know whether they are practising informed consent in a consistent fashion, then although we can rely on associations like yours, it's not enough. In this particular instance, responsibility falls to Health Canada, which is responsible for the safety of women, and for product certification and safety. If a high-risk product or instrument is involved, and there doesn't appear to be enough conclusive data, then the precautionary principle has to apply. That would mean more warnings, not fewer.
Do you think that the Health Canada site has improved since 2019? Has it done enough to be considered comparable to an organization like the Food and Drug Administration, the FDA?