I will answer that question in English, for clarity's sake.
It gets back to this question, which is a legislator's question: what amount of detail do you need in the act versus follow-through in the regulations?
We felt that the general provisions in the act, and we would deal with all of these...and specificity in terms of what bugs are in or out. Even at level three, not all level threes are we as concerned about. Tuberculosis we're not as concerned about as we are with some other level threes.
So that will be the process of the development of the regulations. As the witnesses said earlier about the need to be flexible in what's in and what's out, I can--