Medizone Intl. (fka MZEIQ)

[Zeppo]

This hydrogen peroxide issue is material information related to the development of a lead product and obviously has caused further delays. Was the peroxide issue listed as part of the original test protocol? Did the EPA not bother to inform Medizone, until just recently, that it had this requirement? Did Medizone ignore an original written protocol? Will Medizone have to repeat all of the EPA required tests to see if it obtains the same results using a registered peroxide solution? What kind of a chemical composition difference could there be between a registered and a non-registered solution? Is it a proof of purity issue?