NanoViricides Inc. (NNVC)

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The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation,cosmetics, emitting devices (ERED), and veterinary products.

source: wikipedia

There is a lengthy/expensive Development and Approval process for drugs.

If a toxic drug is meant to treat symptoms or conditions like pain, boredom and stress how does the drug regulatory body or the DOJ determines which drug gets to bypass the development and approval process and which will not? In essence, just how does the regulatory body picks winners and losers or is it the DOJ who has the final word? Rule of men or rule of law?

NanoViricides, Inc. is moving FluCide through the lengthy/expensive Development and Approval process as required by law. Above all, FluCide is low-toxicity and it goes to destroy the root cause of the problem, a virus, in a matter of hours. We also know that FluCide has been effective in 6000 animals (latest figure). Why can 't we get at least a limited license to try our therapeutic drug in the market, at the end of GLP BASi "tox and safety studies"? Just think the money and time that could be saved, the lives that could be saved if we were able to "bypass" the regulatory body, just like toxic Marijuana, straight to market. The money saved could be employed to quickly advance DengueCide, HIVCide and expand the cGMP plant capacity.