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Hokie360

Joined: 08/26/2006 Posts: 17911
Likes: 7206


Keep in mind how much of that would actually be related to safety.


Some of that time savings is achieved by prioritizing the review, not truncating it. If CDC prioritizes the review by putting it queue ahead of other trials submitted earlier, safety is not effected; i.e. same level of review is done. Downside is that the other drug is not reviewed as fast.

If a company queues up manufacturing ahead of final approval, safety is not effected. But the company has a financial risk if they invest in manufacturing something that doesn't end up being approved.

(In response to this post by HokieForever)

Posted: 07/15/2020 at 10:15AM



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Current Thread:
 
  
The report on the moderna vax candidate trial -- ColoVT82 07/15/2020 06:20AM
  If I was over 70, yes I would ** -- HokieHutch 07/15/2020 09:50AM
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  Point of that statement is vaccines in the past -- HokieForever 07/15/2020 09:48AM
  Snake bringing the facts to the argument. ** -- RoswellGAHokie 07/15/2020 09:43AM
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  They could call it Sanguelto ** -- mancunian 07/15/2020 09:02AM
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  The condition known as "hot dog fingers" ** -- `lag 07/15/2020 08:42AM
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