Yes. The system we have in place, I would say, is robust enough for the department to conduct risk assessments based on the information we're receiving through medical device incident reporting. Manufacturers are mandated to do this, and hospitals are as well. Not only are the manufacturers mandated to do this, but there are also conditions imposed on their licence, whereby they need to report on cases of breast implant cancer.
With all of this information, I believe the department is really in a position to conduct risk assessments. I would say this is highly comparable to other regulators in the world.