I'm not sure what Rod considers 'rapid'. The last timeline I remember (which assumed FDA approval in about the Jan/Feb timeframe) had Aethlon completing the safety study by year end, submitting the data, and starting clinical trials in support of a PMA by mid 2014. IMO that is not rapid and as others have suggested, it will be a long time before we see substancial PPS gains (coming from US testing that is). There is still hope that Medanta will approve full use and that would be something we can all celebrate.
Craig2, Good post! AEMD is definitely on the right track finally. We shall see is sage advice. Others will wish they had your fortitude. Regards RTYME24FUN (thanks to JJ and company)