I do actually agree with every aspect of your projected forward looking viewpoint, in regards to third party combination dendritic cell treatment manufacture.
BUT how will you, as an NWBO investor benefit ? Are they not separated out standalone entities now ?
Certainly Advent will be inspected to see that the process they will be using correctly manufactures per the submitted CMC section of the MAA,
There are also inspections of sites to verify GCP (Good Clinical Process), but more importantly as a QA check on the records.
What I do not know is LC;s question. Do they verify that the trial manufacturing sites used a process that is the same as the process described in the CMC section? They have to have some way of insuring they do, but do not know if that is a site inspection.