Public Health and Medical Professionals for Transparency (PHMPT) is a non-profit group of Doctors, Health Experts, Scientists, and Journalists (link below), who are demanding answers from the FDA. The group has filed a legal motion (link below) requesting that Pfizer and Food and Drug Administration (FDA) safety data be released to the public.
In the name of transparency, the group stated the importance of public access to the data used to prove that the Pfizer’s COVID vaccine was deemed “safe and effective.” The motion stated the following...
47. The public debate is unlikely to be settled without full disclosure of the data and information underlying the FDA’s conclusion that the Pfizer Vaccine is “safe and effective.”
48. Given the widespread and ongoing public debate, the medical and scientific community and the public has an immediate need to review the data and information underlying the licensure of the Pfizer Vaccine. Public disclosure of this information will inform this ongoing public debate.
49. There is also an urgent need for the public to have immediate access to the data and information underlying the licensure of the Pfizer Vaccine because, over the objections of many, this product is being mandated to individuals across the country by the federal government. Local governments, public and private employers, universities, schools, and various other institutions, and many are expected to follow suit [written prior to Senate mandate repeal and Appeals Court injunction].
50. During a time when COVID-19 vaccine mandates are being implemented over the objection of those that have questions about the data and information supporting the safety and efficacy of the Pfizer Vaccine, and individuals with these questions are being expelled from employment, school, transportation, restaurants, entertainment facilities, and the military, the public has an urgent and immediate need to have access to this data. The urgent need for the public to review this data is heightened by President Biden’s recent announcement of vaccine mandates for millions of Americans, including employers with 100 or more employees, federal employees, and employees of federal contractors.
Legal Motion link:
https://phmpt.org/wp-content/uploads/2021/10/001-Complaint-101021.pdf
Public Health and Medical Professionals for Transparency link:
https://phmpt.org/?fbclid=IwAR28HiaHmitDfuff7f9VFCz4HIaDTnw1u_3icqEqfmOAaDueYBzfWp1nMZ4
The FDA Response to the Motion:
"... by the time of the Court’s status conference on December 14, 2021, FDA anticipates that it will have produced to Plaintiff more than 3,000 pages of responsive materials. In light of FDA’s assessment, on December 1, 2021, undersigned counsel informed Plaintiff’s counsel of FDA’s updated proposed processing schedule (as set forth here and below) and asked if Plaintiff would be amenable to the proposed schedule. As of the time of this filing, Plaintiff has not indicated whether it would accept this proposal...
Moreover, FDA will have completed processing and production of four items on Plaintiff’s Priority List, items 1 - 8.
FDA’S UPDATED PROPOSAL FOR A PROCESSING SCHEDULE
In addition to the December 13 production, FDA expects to be able to produce the next three items on Plaintiff’s Priority List (items 2 -4) before the end of January 2022. FDA proposes to produce the below records to Plaintiffs according to the following schedule:
• Thursday, December 30, 2021: FDA proposes to produce publicly releasable information from Plaintiff’s priority item #2 – CRF files for site 1081 (approximately 3,380 pages).
• Tuesday, January 18, 2022: FDA proposes to produce publicly releasable information
from Plaintiff’s priority item #3 – CRF files for site 1096 (approximately 2,937 pages); and
• Monday, January 31, 2022: FDA proposes to produce publicly releasable information
from Plaintiff’s priority item #4 – CRF files for site 1128 (approximately 3,452 pages).
If the Court adopts this schedule, by the end of January 2022, FDA will have produced publicly releasable information from more than 12,000 pages of records and 10 unpaginated .txt or SAS data files. Moreover, FDA will have completed production of seven of the first eight items on Plaintiff’s Priority List, items 1-8.
Because FDA has not yet had an opportunity to assess the amount of time it will take to process other records responsive to Plaintiff’s FOIA request, following the January 31, 2022
production, FDA proposes to make one production at the end of each subsequent month totaling a minimum of 500 pages. FDA’s general estimate is that it takes approximately 8 minutes per page to review records for a FOIA production
FDA Response link:
https://www.sirillp.com/wp-content/uploads/2021/12/FDA-Brief-and-Appendix-e3999de9aee38921cd4fbb035c33e304.pdf
A monopoly on medicine and the Glabalists' ruthless attempts to rule over our bodies and minds in order to mentally enslave humanity with AI Censorship Technology.
This is the "endgame" if we allow our own enslavement to the ruling class "Globalists" who program the AI for implementation of whatever plans that they deem "essential."
Note: According to Dr. Berg, entering and remaining in a state of ketosis is how our bodies are designed to be. It causes the body to create uric acid which acts as such a powerful antioxidant that it's akin to scrubbing your kitchen sink with bleach.
Of course the phony 'Globalist' "Healrh Experts (the new priesthood in the modern-day 'science' religion) tell us that it's bad for our health; it prevents disease- their Big Pharma profit generator!
Follow the 💰
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With all of the talk about 'cases' being on the rise; 'waves' of 'surges', 'getting over the curve', and 'trust science'; one must question the sources of this COVID research data so that we will be able to make informed decisions from learning the facts.
As a COVID Activist, it is important to share the facts in order to educate the public so that misinformation from 'Big Pharma', and powerful investors in their numerous corporations can stop misleading us for their own profits.
Vaccine and pharmaceutical revenues worldwide totaled 1.25 trillion U.S. dollars in 2019 and tends to be a primary investment of the world's super-rich, like Bill Gates. Mr. Gates has stated that vaccines have been more profitable for him than Microsoft ever was.
COVID control is based on fraud and greed.
This is what ’the science’ is actually telling us:
1) According to the CDC and scientific method (source link below), there is ZERO valid proof of the virus (SARS-CoV-2) that was declared (unscientifically) to cause ...
During the South Carolina Senate Medical Affairs Ad-Hoc Committee meeting, University Medical Research Professor, Dr. Buckhaults, M.D., is alarmed about the results of his medical research findings and health risks posed by the COVID vaccines. He reports the following:
"The Pfizer vaccine is contaminated with plasmid DNA, it’s not just mRNA,”
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