That's fair enough.
Mr. Graham, along the same line of questioning, you talked about accepting products that have already gone through a regulatory process. I just want to make sure I heard you correctly. Are you suggesting that if the CFIA were to lay down a framework such that if you checked off all of these pieces, and they've been done in country X, the industries would then simply be accepting and say that's the baseline they'll deal with. That would then be where we would look at those products, rather than constantly bringing a new product and saying it doesn't quite fit the framework but it's done by reputable labs, so isn't it okay?
Clearly what happens is this. If you were to say let's open it up to overlapping jurisdictions, which I don't disagree with, by the way, to a certain degree.... There are certainly accepted places where the science they do is equal to ours or the same as ours, maybe even more than ours, or maybe more “comprehensive”, in a way, if I can use that term. Would that be the framework that most industries would have to agree to? There would be give and take with the CFIA, I think, the government, and the industry groups, versus just simply saying this product is really safe, so we should add that to the list. How do you see that framework being developed?