Dear KMAG: 20211206 Joe Biden Didn’t Win ❀ Open Topic

FauXi  Mengele

FauXi was NEVER as ‘benign’ as Victor Frankenstein. Remember FauXi’s WIFE is in charge of BIO-ETHICS @ NIH

“CHRISTINE Grady, who heads bioethics at the National Institute of Health Clinical Center, married Dr Anthony Fauci in 1985.”

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From the FDA’s own website, check out this page talking about the “Joint Leadership Charter” between the FDA and NIH to conduct biomedical research for new treatments and therapies:

Purpose

The need for enhanced collaboration between NIH and FDA has never been more pressing, given new scientific opportunities in translational research, new public health challenges, far-reaching economic changes at the national and global level, and fundamental changes to the U.S. health care system. The National Institutes of Health (NIH) and the Food and Drug Administration (FDA) share a common goal of advancing public health by promoting the translation of basic and clinical research findings into medical products and therapies. The agencies are complementary in their roles and functions—NIH supports and conducts biomedical and behavioral research and FDA ensures the safety and effectiveness of medical and other products.

Function

The Joint Leadership Council works together to help ensure that regulatory considerations form an integral component of biomedical research planning, and that the latest science is integrated into the regulatory review process. Such collaboration and integration advances the development of new products for the treatment, diagnosis, and prevention of common and rare diseases and enhances the safety, quality, and efficiency of the clinical research and medical product approval enterprise. The formation of the Leadership Council represents a commitment on the part of both agencies to forge a new partnership and to leverage the strengths of each agency toward this common goal.

And then look at this one from the NIH’s own website explaining how drugs get approval in the United States…..and just take a look at who actually does the testing (just like we told you!):

How are drugs approved for use in the United States?

The U.S. Food and Drug Administration (FDA) is the federal agency responsible for labeling medications and supplements. However, the approval process is different for prescription and for over-the-counter medications.

Prescription Drugs

The FDA must regulate and approve new prescription drugs before they can be sold to the public. In 2011, the last year for which information is available, the FDA approved 35 new drugs for use by the general public.1 Although this number may seem small, the approval process for drugs is extensive.

The manufacturer or sponsor follows a series of important steps, through animal studies and clinical trials in humans, to ensure that the medication is safe, does what it claims to do, and will provide a health benefit. Testing is performed first in laboratories and on animals to determine that the drug is safe and try to understand how the drug might work in humans.

“Clinical trial” is the scientific term for a test or study of a drug or medical device in people. These tests are done to see if the product is safe and effective for people to use.

Sometimes, multiple trials are completed to measure the effectiveness of a particular medication. Participants in the studies are often followed over a period of time. For comparison purposes, some are given a placebo, an inactive or “dummy” medication, while others are given the actual drug. The NICHD and other institutes of the NIH help conduct and support the research but are not involved in the approval or labeling process.

The clinical trial phase can take years to complete. However, once research has shown that the drug is safe and useful, the FDA typically reviews and either approves or denies an application for a new drug within 6 months.

So despite the “fact checkers” it’s actually true that the NIH does all the clinical research for the FDA and then the FDA just rubber-stamps it in the end.

And it’s true that Fauci’s wife has a very high up position in the NIH.
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.https://welovetrump.com/2021/09/06/did-you-know-faucis-wife-is-the-chief-of-bioethics-at-the-nih-clinical-center/
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“… it’s actually true that the NIH does all the clinical research for the FDA and then the FDA just rubber-stamps it in the end….”

ERRRRrrrrr not exactly.

👉CORPORATIONS or independent testing labs do the actual testing. (I have been involved in both) The NIH provides FUNDING to research that generated patents.

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The US governments concern for the health of Americans does not play given the FDA has routinely over looked “…significant departures from good clinical practice, such as underreporting of adverse events, violations of protocol, violations of recruitment guidelines, and various forms of scientific misconduct…. or submission of false information… The FDA does not typically notify journals …nor make any announcement intended to alert the public about the research misconduct that it finds. The documents the agency discloses [FOIA] tend to be heavily redacted. As a result, it is usually very difficult, or even impossible, to determine which published clinical trials are implicated by the FDA’s allegations of research misconduct.” — Research Misconduct by the US Food and Drug Administration

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In an article for Slate, study author Charles Seife said the FDA repeatedly hides evidence of fraud from both the public and trusted scientific advisers. In at least one case, falsified data in a trial comparing chemotherapies led to a patient’s death.

Nor does concern for public health play given the USDA recent conduct. The Government Accountability Project – “Shielding the Giant, USDA’s ‘Don’t Look, Don’t Know’ Policy” report shows the USDA routinely hid the fact they KNEW Con-agra was shipping E. coli O157:H7 laced meats. It wasn’t until John Munsell forced the issue that the extent of the problem was finally disclosed to the public. Unfortunately the damage was already done to the reputation of farmers and the Ag Cartel dominated USDA/FDA and World Trade Organization got their much wanted Food Safety Modernization Act past Congress.