It looks like you're using an Ad Blocker.
Please white-list or disable AboveTopSecret.com in your ad-blocking tool.
Thank you.
Some features of ATS will be disabled while you continue to use an ad-blocker.
originally posted by: mblahnikluver
a reply to: HawkEyi
They want 55 years to cover up their lies!!!!!
originally posted by: detroitnative
I asked a simple question on an ABC News forum about Gavin Newsom. Where is he and why is he still in hiding. Comment was removed. Totally innocent question but we know why it was removed.
The guy got his booster and went straight into hiding. Scuttlebutt is he has balls palsy and his face is all contorted. All he needs now is a fiddle and California burning.
originally posted by: interupt42
a reply to: MetalThunder
However what is those documents that poses a National threat?
It took the FDA precisely 108 days from when Pfizer started producing the records for licensure (on May 7, 2021) to when the FDA licensed the Pfizer vaccine (on August 23, 2021).
...329,000+ pages of documents Pfizer provided to the FDA to license its vaccine...
The FDA granted full approval for Pfizer-BioNTech's COVID-19 vaccine on August 23, 2021, under the label Comirnaty.
Earlier this month, a now-former employee of Ventavia Research Group, one of the companies contracted with Pfizer to run its Phase III vaccine clinical trials, made allegations that raised questions about the data submitted before Comirnaty received FDA approval.
Brook Jackson, a former regional director for Ventavia, told the British Medical Journal that her 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."
After Jackson notified Ventavia of these issues, she emailed a complaint to the FDA and was fired within hours.
According to investigative reporter Paul Thacker, the FDA did not inspect Ventavia's trial sites even though it was alerted to the issues.
Ventavia has since said it is investigating the allegations.
In a statement to the Epoch Times, the FDA declined to comment on the Ventavia matter but said it "has full confidence in the data that were used to support the Pfizer-BioNTech COVID-19 vaccine authorization and the Comirnaty approval."
.....“Negligence,” yeah. Funny how China managed to unleash two plagues on the world from its virus research labs through “negligence.” The piece also mentions another Chinese bat researcher:
In 2017, the Chinese state-owned Shanghai Media Group made a seven-minute documentary about Tian Junhua, entitled “Youth in the Wild: Invisible Defender.” Videographers followed Tian Junhua as he traveled deep into caves to collect bats. “Among all known creatures, the bats are rich with various viruses inside,” he says in Chinese. “You can find most viruses responsible for human diseases, like rabies virus, SARS, and Ebola. Accordingly, the caves frequented by bats became our main battlefields.” He emphasizes, “bats usually live in caves humans can hardly reach. Only in these places can we find the most ideal virus vector samples.”
One of his last statements on the video is: “In the past ten-plus years, we have visited every corner of Hubei Province. We explored dozens of undeveloped caves and studied more than 300 types of virus vectors. But I do hope these virus samples will only be preserved for scientific research and will never be used in real life. Because humans need not only the vaccines, but also the protection from the nature.”
The description of Tian Junhua’s self-isolation came from a May 2017 report by Xinhua News Agency, repeated by the Chinese news site JQKNews.com:
The environment for collecting bat samples is extremely bad. There is a stench in the bat cave. Bats carry a large number of viruses in their bodies. If they are not careful, they are at risk of infection. But Tian Junhua is not afraid to go to the mountain with his wife to catch Batman.[SIC – LP]
Tian Junhua summed up the experience that the most bats can be caught by using the sky cannon and pulling the net. But in the process of operation, Tian Junhua forgot to take protective measures. Bat urine dripped on him like raindrops from the top. If he was infected, he could not find any medicine. It was written in the report.
The wings of bats carry sharp claws. When the big bats are caught by bat tools, they can easily spray blood. Several times bat blood was sprayed directly on Tians skin, but he didn’t flinch at all. After returning home, Tian Junhua took the initiative to isolate for half a month. As long as the incubation period of 14 days does not occur, he will be lucky to escape, the report said......
.....Then last month a bunch of emails, uncovered by a lawsuit from the so-called White Coat Waste Project, returned the ball right back over the net. They comprised an exchange between the American virus--hunting foundation, the EcoHealth Alliance and its funders in the US government. The scientists discussed collecting viruses from bats in eight countries including Burma, Vietnam, Cambodia and Laos between 2016 and 2019. But to avoid the complication of signing up local subcontractors to their grants in those countries, they promised to send the samples to a laboratory they already funded. And where was this lab? Wuhan.
Some of the emails talk about sending data, not samples; but some talk repeatedly about sending actual samples. ‘All samples collected would be tested at the Wuhan Institute of Virology,’ reads one from 2016. Another in 2018 even talks of sending bats themselves. The emails make it clear that Wuhan scientists would sometimes be working in the field alongside their US colleagues.......
Beware of the deceptions specially when we humans has been forced to take this experiment to have any participation in every aspect of life, they lie to us, they are killing us and we are forced to be nothing but an experimental rat. Time to sue the government.
originally posted by: Starcrossd
a reply to: marg6043
I found the Court docs linked in the article.. at least, to my admittedly untrained eye it looks legit.
excerpt starting from page 10--
...The FDA has proposed to produce 500 pages per month which, based on its calculated
number of pages, would mean it would complete its production in nearly 55 years – the year 2076.
Until the entire body of documents provided by Pfizer to the FDA are made available, an
12 See 21 CFR § 601.51(e).
13 Reports have recently surfaced that the FDA was aware of concerns about unsound practices in connection with
clinical trials for the Pfizer Vaccine, but that FDA failed to properly investigate these claims.
Page 11 of 14
appropriate analysis by the independent scientists that are members of Plaintiff is not possible.
Would the FDA agree to review and license this product without all the documents? Of course
not. These independent, world-renowned scientists should be provided the same forthwith.
The entire purpose of the FOIA is to assure government transparency. It is difficult to
imagine a greater need for transparency than immediate disclosure of the documents relied upon
by the FDA to license a product that is now being mandated to over 100 million Americans under
penalty of losing their careers, their income, their military service status, and far worse.
It took the FDA precisely 108 days from when Pfizer started producing the records for
licensure on May 7, 2021,14 to when the product was licensed on August 23, 2021.
15 We assume,
as the FDA has stated, that it conducted an intense, robust, thorough and complete review and
analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for
licensure. The FDA now has an equally important task of making those documents available to
the Plaintiff in this case and the public at large in at least the same timeframe.