Love your post,
re “suspect backroom discussions between the FDA and Mesoblast have been ongoing since August 13th. If the mechanism for monitoring quality and potency of MSC’s really is a stumbling block, it needs to be resolved.”
im sure this has come up over the course of rolling submission, pre dated to the 13th, you would assume.
re markers, yes, let’s hope that these are what they seem, that is, a scientific and unbiased indicators.
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