$10 by Xmas 2021, page-6

I think the point here is that getting access to non-FDA approved treatments or drugs on compassionate grounds is by no means guaranteed and can be a challenging process...not ideal for burns victims, as treatment is urgent. So an FDA approval not only clears this hurdle but it also acts as a rubber stamp from CDER that the treatment works and that it's benefits outweigh its known risks...so, whilst the degree to which AVH will be able to leverage off this is open to debate, I think I would prefer my child to have a potential max of 2 spray on treatments with a better aesthetic outcome than a potential 5 invasive and painful treatments, with almost certain disfigurement/scarring. Hospitals/Clinicians should, on balance, embrace this also as it saves them time/money...the cells can be ready to spray on in 30 minutes and the patient spends less time occupying a hospital bed during recovery. Win-Win, I'd say! Biggest risk (IMO) is management execution.