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Judge Gives FDA Just Over 8 Months to Produce Pfizer’s Safety Data
The Epoch Times ^ | January 7, 2022 | By Mimi Nguyen Ly

Posted on 01/07/2022 5:00:20 AM PST by redguyinabluestate

A federal judge on Thursday ordered the U.S. Food and Drug Administration to produce, at a rate of 55,000 pages per month, the documents it relied on to license the Pfizer-BioNTech COVID-19 vaccine.

The rate of 55,000 pages a month would mean the FDA has just over eight months to fully produce all of Pfizer’s pre-licensure safety data. That is much faster than the 500 pages-per-month rate the FDA proposed in December 2021. That rate would have effectively given the agency roughly 75 years to fully produce the data, Aaron Siri, a lawyer working on the case, previously observed.

(Excerpt) Read more at theepochtimes.com ...


TOPICS: Front Page News; News/Current Events
KEYWORDS: 54to36; covidtruth; fda; federalistsociety; fortworth; markpittman; marktpittman; ndtexas; pfakevaccine; pfizer; trumpjudge; vaccines
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1 posted on 01/07/2022 5:00:20 AM PST by redguyinabluestate
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To: redguyinabluestate

They somehow make it sound like a serious challenge to produce 55,000 pages per month. Whoo Boy! Think of all the typing!!! Actually, the pages are digital, they are in an archive, and you just need o push a button. Hand over the pages.


2 posted on 01/07/2022 5:05:22 AM PST by ClearCase_guy (The experts are liars. The conspiracy theorists are the people who have figured out the Truth.)
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To: ClearCase_guy

It’s all the redacting that takes time...


3 posted on 01/07/2022 5:07:40 AM PST by HYPOCRACY (This is the dystopian future we've been waiting for!)
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To: ClearCase_guy

Hand over the memory sticks.

8 months is Deep State continuing to laugh its a$$ off at us.


4 posted on 01/07/2022 5:09:47 AM PST by mewzilla (Those aren't masks. They're muzzles. )
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To: HYPOCRACY

gotta crank up the black ink factory. Most pages will be solid black with redactions


5 posted on 01/07/2022 5:10:25 AM PST by Josa
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To: redguyinabluestate
Eight months?

Pfizer needed to have it published BEFORE they were given the Emergency Use Authorization.

6 posted on 01/07/2022 5:10:51 AM PST by T.B. Yoits
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To: redguyinabluestate

This nation suffered greatly because people cannot separate ideas in their head and they conflate one thing with another. Individuals are innocent till proven guilty, but government and large pharmaceutical companies are guilty until proven innocent. We need to figure this out and begin holding the establishment accountable for their greed and avarice.


7 posted on 01/07/2022 5:21:47 AM PST by freedomjusticeruleoflaw (Strange that a man with his wealth would have to resort to prostitution.)
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To: redguyinabluestate
...a federal judge...ordered...
8 posted on 01/07/2022 5:22:14 AM PST by ComputerGuy (Heavily-medicated for your protection)
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To: ClearCase_guy

ClearCase_guy wrote: “They somehow make it sound like a serious challenge to produce 55,000 pages per month. Whoo Boy! Think of all the typing!!! Actually, the pages are digital, they are in an archive, and you just need o push a button. Hand over the pages.”

That would be a violation of the law. Each page, by law, must be reviewed. Proprietary and private information must be redacted. Takes time.


9 posted on 01/07/2022 5:23:07 AM PST by DugwayDuke (Most pick the expert who says the things they agree with.)
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To: redguyinabluestate
Not sure if there will be many redactions, have to just wait and see. I mean, the only thing we have to go on is the previous Pfizer vaccine contract.


10 posted on 01/07/2022 5:23:47 AM PST by C210N (Everything will be okay in the end. If it’s not okay, it’s not the end.)
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To: SeekAndFind

As predicted.


11 posted on 01/07/2022 5:26:30 AM PST by DugwayDuke (Most pick the expert who says the things they agree with.)
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To: DugwayDuke

Then, let’s wait at least 8 months before we force anyone to take the vaccine.

By then, hopefully, we might have others ( like Novavax ) we can compare data with.


12 posted on 01/07/2022 5:35:30 AM PST by SeekAndFind
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To: redguyinabluestate

55 thousand pages a month?

What is in that jab?


13 posted on 01/07/2022 5:39:42 AM PST by just me (Trade your liberty for temporary safety. I will keep mine. My family doesn't fly a white flag.)
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To: redguyinabluestate

There should be nothing redacted. This is an agency about public safety (presumably). There is no BS methods and people that should be redacted. They should not even be given time. All information should be provided upon request. They are stalling for time to hide things not provide them.


14 posted on 01/07/2022 5:43:37 AM PST by pas
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To: T.B. Yoits

BINGO !!!! They should have been able to do a complete data dump in less than 24hrs. FDA already has the data. Any delay is just simple obstruction. Real question is, did FDA actually read the data. Actual true, honest, complete review could/should have taken 6 months or more. Review cycle was what, less than 6 DAYS??


15 posted on 01/07/2022 5:53:41 AM PST by OHPatriot (Si vis pacem, para bellum)
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To: redguyinabluestate

Right before the mid-terms...


16 posted on 01/07/2022 6:09:00 AM PST by null and void (81 million votes ≠ 81 million voters)
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To: ClearCase_guy

At the same time, the company thinks we are making informed consents without any information.


17 posted on 01/07/2022 6:19:57 AM PST by CodeToad (Arm up! They Have!)
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To: pas
I'm not an expert on this but I understand that drug companies submit trial data already deidentified as a part of their data package to the Feds. Identity of individuals is not consequential to the data analysis. This type of data could be released in days I suspect.

What is consequential are the technical aspects, which are dealt with statistically. The bulk of the data package should be largely available electronically with little if any redaction.

A separate part of the affected data package would likely deal with composition and production data that is likely to be heavily redacted via proprietary or other business claims. This is the type of information that would be contentious to publicly release and vulnerable to being tied up in court to validate claims of confidentiality.

If I have missed on any of this, please correct me. Perhaps some of the points can be described better as well.

18 posted on 01/07/2022 6:21:14 AM PST by Hootowl99
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To: ClearCase_guy

It takes time to edit out the incriminating data


19 posted on 01/07/2022 6:25:25 AM PST by ChildOfThe60s (If you can remember the 60s.....you weren't really there..)
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To: redguyinabluestate

What’s the odds anyone at the FDA actually read through ~440,000 pages of documentation to make their decision?

March 30th, 2020 the U.S. Department of Health & Human Services (HHS) started a program they coined “Operation Warp Speed,” (OWS) in an attempt to expedite a COVID-19 vaccine.

Pfizer provided the FDA with ~440,000 pages of documentation to base the EUA on in 9 months. The FDA EUA was granted on 11 December 2020... yet they say it would take 75 years to gather all the documentation.

If that were the actual case, they wouldn’t be able make their EUA decision until 2097 because you’d need all that documentation to make the decision.

Typical government.. reality here is they have all the documentation but had already made up their minds on the EUA.

Now they need 75 years to read the documentation to see if they made the right decision which to the obvious is no and all those involved will be dead in 75 years so no one can be held accountable.

I think the Republicans should produce a Reparations Bill for all those harmed by the jab forced upon them by all the government(s) Federal, State and Local, Corporate CEO’s etc, and the families of these government(s) Federal, State and Local, Corporate CEO’s etc should be financially responsible for all individuals harmed by the jab and include surviving family members and descendants.

Be fun to watch the left..


20 posted on 01/07/2022 6:25:47 AM PST by maddog55 (The only thing systemic in America is the left's hatred of it!)
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