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Charmaine Gittleson Speaks on FDA Feedback, page-2

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    Great summary. Charmaine is clear that the FDA is fully supporting this research and allowing fast track of parallel toxicology study reduced from 12 months to 9 months also permitting higher dose. The outcome could not have been better. One more trial before commercialization.. Rerate is imminent.
    Last edited by monti901: 03/06/21
 
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