I'd like to discuss a proposal with you:
That, pursuant to Standing Order 108 (2), the Committee undertake a study to follow up on the improvements that have been put in place to tighten Health Canada's rules and improve oversight of medical devices (breast implants) in 2018 and assess the feasibility of establishing a central breast implant traceability registry that would make it mandatory for practitioners who implant, remove, or replace breast implants to enter certain data into the registry and that:
a) the Committee hold a minimum of two (2) meetings with witnesses;
b) the Committee report its findings and recommendations to the House;
c) pursuant to Standing Order 109, the Committee request the government to submit a detailed response to the report.
I drafted this motion based on the discussions we had, during which we planned to conduct a number of short studies before June. However, I think this topic merits further attention. The motion for which I gave notice proposed that two meetings be held, but I'd like to increase that number to four.
We've been discussing this topic in this Parliament for many years. Many members, particularly former NDP members, have tabled legislation in an attempt to establish a breast implant registry. Now in 2022, that still hasn't been done despite all those attempts.
As the motion states, the rules have been tightened. In 2006, certain types of silicone breast implants had been approved, and that caused some problems. That explains why the rules were subsequently tightened. It's important that we be able to conduct follow‑up to determine where we stand in 2022. Is what was put in place back in 2018 actually working? We need to hear from witnesses who can discuss their experience with us.
This is crazy. The trouble we've had in this file stems from the fact that the problems, in many instances, emerge 10, 15 or 20 years later. The practitioners in question are often retired or no longer in the picture. Since there's no registry, the women who are dealing with the problems or who are unaware of any potential problems can't verify what was implanted in them. When you know that most problematic implants were introduced during reconstructions, in women who have had cancer, for example, it's important that we be able to resolve this issue once and for all.
We can't presume to know the conclusions and recommendations that will emerge, but we want this study to remain very specific. Otherwise, when studies are too broad, you rarely manage to determine the main recommendation and ensure that it results in a bill or action. Consequently, in this instance, we need to move as quickly and precisely as possible to come finally to the recognition that everything done over the years should have culminated long ago in a single measure, the creation of a registry.
That's more or less what I had to say. I have a 26‑page file that I won't read to you today, but I can answer any questions you have on the relevance of this motion and debate it with all my colleagues.