I would take that bet, except I don't drink.
It will probably last almost an hour, but you will hear a lot more about a future Business Plan, Dilution, Manufacturing, Patents, U.S. Trials in selected hospitals, final application for FDA approval, South American ventures, Singapore ventures, and maybe something about Anthrax/BioTerrorism.
Perhaps enlargement of BOD, or business associates and staff.
I suspect there will be several people who will speak and many are long winded.
Keep in mind that they would NOT hold a Shareholder meting unless they had something worthy of reporting. The timing is very obvious. They knew they had EPA approval, so now is the time to really begin to launch some kind of business plan. They were stymied for the last 3 years waiting for EPA.
Now they can begin the real journey.
Also keep in mind, and this is important, if you area capable of eradication all pathogens and can sterilize a spore pouch, then you are qualified to apply to EPA for Sterilization status. There will be many more trials and hurdles, but this can be accomplished. Our current EPA approval was a GIGANTIC step forward. Many tests can now be done. Sterilization is far more profitable than cleaning hospital rooms.
If there is no reports of C-Diff, or MRSA, etc, then the hospitals don't need to use AS. However, all medical devices need to be used daily and even multiple times per day, for sterilization.
I am holding our for the Autoclave business.
