The more you look at this, the more frustrated you'll get.
The upshot is we can see this, the industry/ medicals/ scientists can see this - why can't the FDA?
Of course the FDA can see this - so why make an example out of Mesoblast?
It comes back to one thing for me - the burden of being the 1st FDA approved MSC product- and the bureaucracy that we have to navigate as a consequence!
MSB to dispute FDA finding in Type A meeting, page-385
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