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Re: HoneyBager post# 171241

Tuesday, 02/27/2024 11:07:50 PM

Tuesday, February 27, 2024 11:07:50 PM

Post# of 175626
Never said otherwise. But in that case (Mayo docs not certified at time of IDE submission) best RDGL can receive is a conditional approval with a check list of items that must be completed to FDA satisfaction before human trials. Likewise for the manufacturing problems with Radiogel. All these issues have to be resolved before FDA will permit human trails. Again, MK is still messing with basic issues that competent management would have put to bed years ago.
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