I have done a little work. I have a colleague who sits three offices away from me, Dr. Blaine Chronik, who's also a Canada research chair. He does a lot of this work for Health Canada.
The reality is there is virtually no harmonization with the EU, or even within North America, on devices, drugs, or even electrical systems. We have the CSA. It's considered one of the stamps of approval internationally. In Europe they have CE. In the United States they have UL, which is Underwriters Laboratories. When we get a piece of medical equipment from the United States and it has UL on it, we have to spend thousands of dollars getting CSA approval before we can plug it into the wall at our university, because those are the provincial and federal standards.
I'm afraid that red tape has a long way to go before it's actually amenable to the exchange of all these things in any kind of seamless manner.