The FDA is going to analyze all the trial data and provide briefing documents to the advisors who will then carefully review them. So, yes, no rush.https://twitter.com/NateSilver538/status/1357493589031452679 …
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it is one of the reasons that I want developers I work with to understand the "why" of what they are working on. if all you know is your toolset you are likely to fail in a way that a subject matter expert could have saved you from if only you had asked.
Thanks. Twitter will use this to make your timeline better. UndoUndo
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