Tuesday, September 30, 2014 1:12:54 PM
http://www.huffingtonpost.com/2014/08/05/big-pharma-ebola_n_5651855.html
All hands on deck! EbolaCide is spearheading NanoViricides, Inc. breakthrough technology and must prove efficacy, just a few weeks ahead, 2014. Signing agreement with BSL-4 lab and validation of our 5kg cGMP Pilot Plant are other immediate goals.
If EbolaCide efficacy is dramatically improved, evidenced by BSL-4 partner testing (likely USAMRIID) that will make FluCide more attractive to BigPharma. On the other hand, people may also start to question why not streamline regulations for FluCide as well? People may start to question, "...I don't want the flu vaccine. I'd rather have the likely low toxicity and effective FluCide." That is what headlines on EbolaCide effectiveness could do to people. The knowledge that there are other options in the event vaccines fail is very enticing.
http://healthimpactnews.com/2014/government-pays-damages-to-vaccine-victims-flu-shot-most-dangerous-with-gbs-and-death-settlements/
Why would the not-so-invisible hand of the FDA impose proof of toxic dose on low toxicity and effective FluCide when FluCide could very well lead away from a life threatening virus and the dangers of vaccines??? http://www.nanoviricides.com/press%20releases/2013/NanoViricides%20Inc%20Reports%20Excellent%20Safety%20Profile%20of%20Its%20Broad%20Spectrum%20anti%20Influenza%20Drug%20Candidate%20FluCide%20in%20a%20Non%20GLP%20Study.html
All hands on deck. Unequivocally, our main objective should be and is to prove EbolaCide's efficacy, just a few weeks ahead, 2014.
How do you like that not so premature enthusiasm?
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