for attentives only … almost 9 hours long ! The U.S. Food and Drug Administration has scheduled a meeting of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) on Dec. 10 to discuss the request for emergency use authorization (EUA) of a COVID-19 vaccine from Pfizer, Inc. in partnership with BioNTech Manufacturing GmbH.
Author Archives: jascally
The Act … Are We Being Prepped ?
Children’s Health Defense
Just a Reminder … You Know, Jog your Memory
Are we still in a pandemic ?… WHOs definition that is