“This 108-day period is the same amount of time it took the FDA to review the responsive documents for the far more intricate task of licensing Pfizer’s COVID-19 vaccine,”
“The entire purpose of the FOIA is to assure government transparency,” they continued. “It is difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse.”
They also argue that Title 21, subchapter F of the FDA’s own regulations stipulates that the agency “is to make ‘immediately available’ all documents underlying licensure of
Szczepionka Pfizer już na etapie badań klinycznych była kontrowersyjna. Ilość uczestników, którzy zmarli i z którymi kontakt został utracony jest co najmniej zastanawiająca.
Trzeba dodatkowo zaznaczyć, że grupa kontrolna placebo dostała możliwość zaszczepienia zaraz po autoryzacji szczepionki.
Czy