[laughs]

... something that I am saying it depends on the context.

We can't standardize.

Uh, but I think ultimately it comes back to standardization removing needless variation.

And so things like concentrations, naming, the way high-risk medications appear in the drug library are all good places to start and good examples where standa- standardization will really improve safety and practice.

But- Again, it's a complex system, and so we need to have that standardization.

We need to have a threshold with which we measure our expectations of how something, how a device performs, and that's where, you know, the AAMI standards that I work with are really important.

Yeah.