I think it is safe to say that if you, among others, toured the facility, the walls of the facility are all integrated. I do not know if FDA will give its stamp of approval on every stage of the cGMP Pilot Plant...??? Next? Moving the equipment into the facility as soon as it arrives at the premises. Then get the equipment/instruments humming to produce (3) identical batches of the FluCide candidate. The FDA will give its stamp of approval at this stage.
I hope GLP tox studies preliminary results will prompt NanoViricides, Inc. to request "Breakthrough Therapy designation". That will be another PR as we get "Fast tracked".