That 10,000 seems a very big stretch listening to his answers......and I doubt would be met imo.
"Blueprints" vs reality and raw material issues.
"It is also worth noting that once cell potency assays are agreed upon with the FDA, provided 3d manufactured Remestemcel-L meets these assay and quality control measures no new trial will need to be conducted as the product is measured to be the exact same, with the same clinical efficacy linked to biomarkers as 2d manufacturing."
Can you reference this from Mesoblast themselves?, as I have seen SI state the exact opposite in a recent video interview.
so this remains to be seen imo.
MSB have "talked" about it for 6 years with language like "finalizing" so again, I remain very skeptical as to why they didn't use 3D already as they stated in annual reports since 2015.
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