I heard two questions. I'll address the R and D commitment piece, and then I can go to the health piece.
For us, as we were discussing, the nature of research and development has changed in Canada. We've had this definition, as you pointed out, since 1987, but research has changed, and the type of research we do now and the type of investments we attract in Canada have changed. They're actually not captured in that definition.
We have companies like ours that bring global investments directly into the country. We have partnerships with biotechnology companies. We have venture capital, which you've heard about. We have acquisitions. We have private-public partnerships. All of these are different types of research and development that exist now and that are not captured in that definition. In fact, a vast majority of the $190 million in Mississauga I spoke to you about doesn't qualify for the SR and ED tax credit, which is what is used to measure that 10% commitment. I would also add that none of our investments in the Montreal Heart Institute qualify for the SR and ED tax credit, even though they are investments directly into this world-class academic research organization.
What I think might be interesting as you deliberate and consider intellectual property and its impact on investment is to actually look at these definitions. Look at how things are measured to ensure that we are capturing the true definition of research. Look at the true way investment is now coming into Canada, because, as you point out, it's very different from what it was in 1987.
In terms of health care and what we mean by tools, we have very good conversations when we bring our drugs to market. We go to the provinces. We submit our medicines for consideration for reimbursement. There are a number of things we consider and that we negotiate with provincial governments. Those are the tools I'm referring to.
Some provinces may have product listing agreements. Some provinces negotiate very well on criteria. For example, you have your drug, and it can do these things, but we would prefer that it come to market after you've tried this drug or only in this subset of patients. There are a number of different ways we have discussions within the health framework on these products coming through.
I would also add, and Declan may want to chime in as well, that when we're looking at what else happens around the world, I don't believe that there's any other industrialized country that uses the argument that it should weaken the IP regime to control health costs. The two usually aren't married.