Replies to post #675374 on NorthWest Biotherapeutics Inc (NWBO)

[Smokey21]

I tend to agree with your explanation of the two phases being necessary, and an RFI pause (if needed). I don’t know this for sure, but it would make sense that the first 80 days are activities that review and validate the data, audit sites, etc…. From those processes would likely come any questions and data requests if things aren’t clear in the application.

Assuming the RFI process isn’t needed, I would imagine they move to Phase II where they probably consider stakeholder input and expert opinions along with considering the risks, benefits, etc., before making the final recommendation on approval.

So, while this is all supposition on my part, it seems logical based on my layman’s understanding of the overall process. Better to assume the 150 days and be surprised if they conclude sooner.