Eli......your "quote" reminds us of the issues of management to seek, identify, and navigate the regulatory process four years ago. Today, what we still don't know is the essence of Medizone's correspondence with the EPA in May. What does the continuous answering of questions mean? Were the questions asked in conjunction with the 160 petri dish tests already submitted or were new tests required? Given the lack of testing in real life hospital situations, how could anyone slight the EPA for asking for more results? It is mind boggling to me why there is no testing in Canada.....outside....of course.....the obvious.
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