Thanks so much for coming back. It's been really interesting to listen to all the testimony, and I really like the fact that there have been some recurring themes.
Following up where Mr. Bossio and Ms. Gladu were going, I think one of the top recommendations is adding some sort of plastic to schedule 1 of CEPA, but how do we do it? Do we do it as plastic? Do we do it as a subset of plastic? Do we do it as plastic waste? Like, what is it that we'd make the recommendation on? I wonder if you could provide a little more clarity on this. I'm not a scientist, to be honest, and I want to be as effective as possible, but I don't want to eliminate the use of....
If we classify “plastic”, does that mean you can't use medical devices that are plastic if we put that under schedule 1 of CEPA? Or does that just allow us to do testing and various different things where it gives us the option to do a whole bunch of things and doesn't mean we are automatically banning anything? I'm wondering if you could clarify that very quickly.