but things have not gone well bro,an ind that took 4 yrs to submit and was changed from a phase 3 to a 2 and fda still couldnt give us the go ahead,i agree with old musky,the problems with ind are the ind itself,to say fda just wants more info about this tech is lunacy,the looked at it and right away there were problems which is why the huge inside dump came at submission which didnt allow the pps to rise,these are facts are they not and we are at subpenny,cmon now