Can I answer?
There are a few answers to that. First, no legal regime is perfect, so your scenario is plausible. The regulations have been designed to ensure that the proponent of the substance provides the government with information that we believe we need to make that assessment. And it is interesting that these regulations have recently gone through an amendment that was the result of a two-year process that involved stakeholders. This is almost unique in the history of the two departments. That two-year process resulted in a consensus set of recommendations from industry, NGOs, and government about the nature of the information that should be provided. So there's a strong attempt to ensure that we address those issues.
Secondly, if in the assessment we say that we're confident that the use you're putting it to right now is safe, but we haven't been able to think about all the other possible uses to which this substance could be put in the future, the act allows us to do what's called a significant new activity notification. It says you can use it for that use, but if you want to use it for something different, you have to go through the whole process again.
And the third point is that if we do get it wrong, we can still assess it again, but then we have to assess it as an existing substance, not through the reverse onus new substance regime. So it's a substance on the market, it's in use. We can still assess any substance we want and determine whether further action needs to be taken.