The FDA is a corrupt organization., page-80

Where are the parents of the children with aGVHD?
Court order is required to make the FDA hand over the approval then and there.

Why do Children need to wait for the trials on the adults to be over?
Is it the system of healthcare for the ones who need quick favor?
When Mesoblast's support for the children are ready, why are the FDA not becoming speedy to let the children access the support?

SI generated some pilot data in adults, then why did the FDA not consider the pilot data a basis for an approval for the children?

SI needs revenue to expand the support from children to adults. Approval for the children would ensure support for children and open fund for Meso to expedite the trials on adults.

All regular meetings between Meso and FDA were for what purpose? If Trial data on adults were mandatory for the children, why did FDA let Meso submit the approval application?

Australian Govt needs to help Meso to secure the approval for the children.
SI sounded too naive to comprehend the FDA's expectations.
Where are real clear experts' comments in the differences between the Fda 2020 version and the Fda 2023?
why did Dr Kaurose fail to explain what SI should have known prior to wasting time and shareholders' funds?

Are there any agencies other than FDA for the Meso to get the approval done for commercial launching while all data and paperwork are made ready to be accepted by FDA for approval?