I remember tons of data and discussion about marke
Post# of 30027
What I'm not clear on is how hard is regulatory approval for diagnostics? I believe the original plan was to start only with phrama trials, which would mean faster approval, and it seems that is the current plan as well. I read up on it a bit but the FDA documentation is massive and complex, so I'm wondering if anyone else knows how easy it would be to get this moving, with 2.0?