Hi all
So the next little 'push' we can expect would be the FDA minutes of the meeting MSB had about the resubmission?
When would people expect to see these released - as this should shed light on the 'remaining characterizing issues' that seem to be the only hurdle between FDA approval now?
Appreciate the LTH answering, what must seem like, tedious questions.
Appreciate it.
Upcoming Newsflow & Re-rate Estimations, page-44
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