but because the CYDY team lacks experience present

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but because the CYDY team lacks experience presenting information

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Amarex is handling that and they do have experience with many drugs they've handled approved. Now there might not be another company that's handled as complex of a submission as our HIV was.

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nmbr1stckpckr, you must then presume the FDA has done something to make the process more difficult for CYDY, in spite of zero/any specific evidence to the contrary. The totality of the known missteps do not belong to anyone but Nader. - Rubraquercus

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In HIV did Nader ask the FDA to do a combo trial? Did he ask them to insist on 700mg then repeatedly request information from a different trial? In COVID-19 he has done nothing to delay it. If he had insisted on 50 patient interims in both trials then there would be delays.