No, I have not drafted medical device...this is only in the federal sphere in Canada, and I have not done anything in that sphere. Health Canada has not asked me to draft any of its legislation in this area.
There are other jurisdictions. We'd have to look outside of Canada to the United States or Europe. Unfortunately, the United States is not a particularly good model, because that's where many industries are located. I think Canada was a leader in this area but is no longer. Decades have gone by.
Unfortunately, I believe that globally the protection of the public has been reduced. International harmonization means a race to the bottom and lowering the standards. Canada has done that to make it easier to allow drugs on the market.