Hawkbar, They are organising the supply of drug at commercial scale for the rest of the trials. Once the have established OBD they need ti get bigger quantities and also prepare for commercialisation These suppliers need a o be FDA approved.
The factory must be approved. Also they need to do shelf life testing on the commercial supply. All of this needs to be done before FDA approval. Even the packaging and labelling needs FDA approval!
All of their decisions point to a concrete plan to commercialise these drugs. Because YF and LC already know this is going all the way to market.
That’s also born out by the presentations showing forward planning of future trials.
It s really easy to read the roadmap
LC has presented.
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