Republican Sen. Lindsey Graham says he's tested positive for Covid after being vaccinated, and is certain he'd feel worse without the shot
From CNN's Naomi Thomas
Dr. Peter Marks, director of the Center for Biologics Evaluation and Research at the US Food and Drug Administration, said in an interview with the Washington Post Friday that the center will work towards getting Pfizer’s Covid-19 vaccine full FDA approval as quickly as possible. Marks also explained the difference between what is required for emergency use authorization, which all the vaccines currently have, and full approval, saying that “in terms of pages to review the change is an order of magnitude. It’s going from tens of thousands of pages, to hundreds of thousands of pages.”
Marks said that what is normally done for biologic license applications is to have six months of follow-up data on those who received the vaccine in clinical trials. He said that the data from the millions of people who have gotten the vaccine but were not part of trials can’t be used because “we don’t follow all those millions of people in the same manner that we are able to follow people who are enrolled in clinical trials.
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