What I still do not understand is where is the information on the FDA pre approval or final approval of the IND? You have stated it was pre approved but so far there is no where that has been shown. It is not on the FDA web site. When you go to their webpage, you cannot find it. When you go to the Generex / NGIO web site, they make no mention, when you go to the news outlets, it is not there. When you search the internet in general, it cannot be found.

So, doing due diligence as you stated, it cannot be found. So, can you provide your source on where you found that the IND from July was pre approved, so that issue can finally be put to rest once and for all?

Edit: This is really a simple and easy request...