For researchers who were testing Pfizer’s vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety.
A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson , emailed a complaint to the US Food and Drug Administration (FDA). Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails.
Read the full investigation: Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial https://www.bmj.com/content/375/bmj.n…
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Brook also gave an extensive interview with Dr.Fuellmich in the Coraona ausschuss de,session 94.working with an understaffed/unqualified personnel keeping the vials under inappropariate temperature settings. She also had personal intimidations/threats like text messages,phone calls & computer probelms. She also had connection problems while talking live to Dr.Fuellmich & Dr.Fisher.
https://odysee.com/@Corona-Investigative-Committee:5/Session-94-Brook-Jackson:6
If you have trouble with the connection just search for: Corona ausschuss de, then click on:Session 94, Stepping on their feet.