Going back to what was originally there prior to December, or January of this year, it was a set of guidelines where there were questionnaires and surveys for the donor, if living, or if it was cadaveric, of the family, and it went through all the scientific and empirical testing for disease. If it was found to be tainted and not usable, it went through the exceptional distribution clause and there was physician and recipient informed consent.
I think a measure of those three together would give us something that is safe and equitable.