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Saturday, 04/17/2021 10:57:14 AM

Saturday, April 17, 2021 10:57:14 AM

Post# of 232965
Quote from FDA Advisory Philippines:
“ However, while a CSP grants access to investigational drugs, such as Leronlimab THE PERMIT IS NOT INTENDED TO REPLACE THE PRESCRIBED DRUG REGISTRATION PROCESS WHICH INVOLVES A SYSTEMATIC EVALUATION OF EVIDENCE BASED DATA.”

How precisely does CYDY meet the above stated threshold with the data in hand?

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