If I could just pick up on this idea of reverse onus, I think you really hit it on the head. There is essentially a reverse onus that operates already under the legislation in the sense that, for new chemicals, companies have to provide information. The government then makes an assessment, and if they want more information, they get it.
The real key issue in comparing this to REACH is, who do you want to make the assessment? In REACH, they're going to have the companies make the assessment. There's some kind foggy evaluation that the government will make later, but that will be a long time later. You don't know when. In Canada, for new substances, the government makes the assessment when they make the decision, and the companies have to provide the information.
We've kind of started to move into that same paradigm with the announcement on Friday. Clearly, for the first 200 or 500 substances that they're going to work on, that is how it's going to operate. They've identified the schedule they're going to assess these on, industry will need to provide what information it thinks it is going to have to provide, and the government will then make the assessment. We're going to get through that schedule of those 500 top priority substances within three years.
REACH, on the other hand, has a list of substances that may be subject to authorization, which basically is similar to, say, our virtual elimination. In an OECD meeting I went to recently, the Europeans noted that they'll probably deal with 20 of these a year. They're going to take much longer than we will to get through the list of substances. The European official I talked to said the length of time this is going to take isn't something they really publicize. But I think we have a much more efficient way of dealing with this in categorization, and we in effect do have what I'm not sure is technically reverse onus, but in effect it has the same purpose. The government will make the decision, and they'll get the information they need from industry to make it.