Pfizer Phase 3 clinical trial fraud allegations that should be immediately investigated by the FDA

It is in the best interest of all parties to have transparency in these issues in order to restore public trust in the medical community and reduce vaccine hesitancy which are key goals of the CDC and FDA.
 
For example, Dr. Peter Marks recently stated:

“We do have a problem with vaccine uptake that is very serious in the United States and anything we can do to get people more comfortable to be able to accept these potentially life-saving medical products is something that we feel we are compelled to do,” said Dr. Peter Marks, director of the Center for Biologics Evaluation and Research.

There are two things Dr. Marks can do to achieve his goal:
 

1. He can have an open discussion with the people who he alleges are the main spreaders of “misinformation.”

2.  

3. He can open an official FDA investigation into allegations of fraud in the Pfizer trial and produce a written report responding to each allegation.

Dr. Marks refuses to do #1. I understand why he won’t: the data isn’t supportive of the government narrative so he’d lose the debate very badly. This is why nobody at the FDA, CDC, or NIH will talk to any of my colleagues.
 
But #2 is critically important. If there is fraud/ willful misconduct, the liability protection is removed. If the FDA is truly working for the people, these allegations must be investigated.