The inside job of Janet Woodcock at the FDA and how she fixed the requirements for EAU by waiving toxicity testing for the jab in May 2020. This is evidenced in the contracts the NIH, FDA, CDC and their associated agencies made with the drug companies to produce the jabs. It clearly stated that after having closed door meetings the drug companies she would omit toxicity testing due to results from testing done on MERS and 1 other one which evades my thoughts at the moment, but neither of them were mNRA based therapies. Then Trump announced the creation of Operation Warp Speed (OWS) which ran from May 15, 2020 – February 24, 2021 (285 days). She was hand-picked by him to head up the team to develop the monoclonal antibodies that would be able to be used in the jab under EAU in early May 2020. She left the FDA and joined OWS. She made a video in early November 2020 while working on the project and in that video she claimed that since she was no longer part of the FDA, there would never be any conflict of interest as she would not be part of the approval process. (LIAR) Then within a very short period of time she claimed to have found safe enough monoclonal antibodies that could be used by December 10 of 2020 then left OWS within a week afterwards. Just hours after U.S. President Joe Biden was inaugurated, Janet Woodcock, M.D., officially took the reins at the FDA on January 20, 2021 as spointed by Biden. Then on August 23, 2021, the U.S. Food and Drug Administration approved the first COVID-19 vaccine. Now keep in mind that while under her watch with the FDA she waived toxicity testing requirements in early May, 2020, left the FDA immediately thereafter and joined OWS and developed the jab and then left OWS and was reappointed to the head of the FDA and then very same toxic substance she enabled to be made for use under EAU was approved by her/FDA. (which was a major conflict of interest) Now on August 23, 2021, Janet Woodcock reportedly was then srated to be out of the race for permanent FDA commissioner and Biden had until November 15, when Woodcock's term as acting Commissioner was to expire, to nominate a permanent head. -- Before all this happened, Janet Woodcock while heading the team at the FDA to approve medicines and drugs had denied the approval of use for mNRA on 4 or 5 occasions from 2004 TO 2016 as they were found to be to toxic for use in humans as trials on animals had shown they were lethal. IN 2016 Moderna raised a boatload of money and used it to further push the use of mNRA and said that they understood that too much of it used at once as a full dosage was too toxic and they would develop a dosage delivery system that would lower the initial dosage amount and then give a secondary lowered dosage amount to try to lessen the amount of toxicity of the drug. Thereafter she did what she did to get the drug approved under EAU. They all knew exactly what they were doing and this all started back before SARS. They gain of function research had been ongoing for years and the creation of covid in a lab was needed to create a crisis so that the mNRA could find a way to be unleashed onto the world. Fun fact -- Janet Woodcock while with the FDA had posted her research details and within them is said that the FDA and the Rockefeller University would be providing the cell lining walls from fetuses embryo's for the jabs (if I remember properly was for the Pfizer jabs) to be produced. Follow the money!