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Tuesday, January 16, 2024 8:13:35 PM
read and COMPREHEND.....
Fast track your marketing authorisation
Applications can be fast tracked if there is compelling evidence of benefit in a public health emergency or if there is a shortage of supply of an essential medicine that has been verified by the Department of Health and Social Care (DHSC).
Seriously people stop with the false hype.
GBM is terrible.
It is not, however, a public health emergency.
DCVax does not fall under the categorization of this fast track program at all. Period. End of story.
Stop creating false and absurd expectations.
150 day review. 60 day RFI. Subtract 30 days for optimistic efficiency. That’s late June timeframe.
That’s what we’re hoping for. Late June. There’s nothing wrong with that. Stop with the bullshit pump theories.
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