The Food and Drug Administration (FDA) is an executive branch agency, the beneficiary of vast legislative powers delegated to it by Congress. It is also …
Food and Drug Administration (FDA)
The Food and Drug Administration (FDA) is an executive branch agency, the beneficiary of vast legislative powers delegated to it by Congress. It is also the repository of powers not delegated by Congress that FDA has usurped beyond the limits of its enabling statute throughout its 68 year history. The Commissioner of FDA sits at the pleasure of the President. The FDA is one of the largest and most powerful federal bureaucracies. It regulates over $1 trillion dollars of goods. The products under its jurisdiction account for 25 cents of every dollar spent by American consumers. FDA has approximately ten thousand employees and 26 district offices across the United States. The United States Attorneys and federal marshals are at its disposal and can obtain search and seizure warrants to be exercised without any advance notice against any company that sells a food, dietary supplement, drug, or medical device in the United States.
To understand how FDA has acquired so much power in a government designedly of limited powers, we have to appreciate the agency’s place in history. Indeed, we have to start with the origins of American constitutional government, 151 years before the FDA came into existence, to appreciate the perversion of the Framers’ plan effected by the modern FDA. We must follow America’s late 18th Century rejection of the arbitrary will of King George III, its embrace of a written Constitution where the law and a system of separation of powers and checks and balances were supposed to prevent the accumulation of tyrannical power in any one set of hands. We must then observe the rise of independent regulatory commissions in the Twentieth Century and how those commissions united legislative, executive, and judicial powers into single hands in violation of our founding principles. We must then come to see how FDA in particular exemplifies the arbitrary rule of people in power over the rule of law.
The Epoch Times published an explosive report today stating that they have received emails that allegedly show that the U.S. Food and Drug Administration (FDA) and National Institutes of Health (NIH) have been quietly studying neurological problems that have appeared in people after they took a COVID-19 vaccine. The report states: Two U.S. agencies have been quietly studying neurological problems that have appeared in people who have had ...
Project Veritas published Part Two of its series on the FDA on Wednesday night which featured FDA Executive Officer, Christopher Cole, speaking about the inner workings of the agency including the FDA’s conflicts of interest, overspending, and why it’s hard for those within the agency to speak out on such abuses. In Part 1, Food and Drug Administration [FDA] Executive Officer, Christopher Cole, inadvertently revealed that ...
Planned Parenthood is promoting a new cartoon ad urging children to take hormone blockers to delay puberty if they believe they are “intersex” or feel confused about their gender. “There’s no one-size fits all puberty experience. If you’re trans, intersex or nonbinary know that you’re not the only one feeling confused,” the narrator of the ad for kids assures. Children who are “intersex” may experience puberty ...
The Canadian Covid Care Alliance, which consists of over 500 independent Canadian doctors, scientists, and health care practitioners, released an in-depth analysis of the Pfizer COVID-19 vaccine claiming that it can do more harm than good to people. According to its website, the Pfizer 6 month data shows that Pfizer’s COVID-19 vaccines cause more illness than they prevent. Also, an overview of the Pfizer trial flaws in ...
A nurse who has worked in the intensive care unit for over two decades is sounding the alarm on the disturbing malpractice she has witnessed and was subjected to in a hospital’s intensive care unit throughout the coronavirus pandemic. As the medical community adjusts to treating the man-made virus, a Chi-com bioweapon, the end of the “state of emergency” appears to have no end. A nurse ...
On November 16, 2021, it was reported that 15 vials of smallpox (variola) were found at Merck’s North Wales, PA laboratory in a freezer. While many people are panicking about smallpox being used as a bioweapon to unleash on Americans, as Bill Gates suggested just a couple weeks ago, the real question is – were there really vials found, or is this to invoke panic, siphon ...
The FDA has asked a federal judge to make the public wait until the year 2076 to disclose all of the data and information it relied upon to license Pfizer’s COVID-19 vaccine. That is not a typo. It wants 55 years to produce this information to the public. As explained in a prior article, the FDA repeatedly promised “full transparency” with regard to Covid-19 vaccines, including reaffirming “the ...
Billionaire globalist Bill Gates has urged world leaders to prepare for an imminent “bioterrorist attack” that will result in a pandemic much deadlier than Covid. Appearing in a Policy Exchange interview with the chair of the Health Select Committee Jeremy Hunt on Wednesday, Gates called for the creation of a new World Health Organization (WHO) body to be formed. Bill Gates was one of the few who warned ...
A whistleblower involved in Pfizer's pivotal phase III Covid-19 vaccine trial has leaked evidence to a notable peer-reviewed medical publication that poor practices at the contract research company she worked for raise questions about data integrity and regulatory oversight. Brook Jackson, a now-fired regional director at Ventavia Research Group, revealed to The BMJ that vaccine trials at several sites in Texas last year had major problems - including falsified data, broke fundamental ...
An FDA vaccine advisory panel on Tuesday voted unanimously 17-0 in favor shooting up kids aged 5-11 with Pfizer’s experimental mRNA injection with panelist Dr Eric Rubin stating, “we’re never going to learn about how safe this vaccine is unless we start giving it.” FDA Committee has approved the Pfizer vaccine Emergency Use Authorization for kids aged 5-11. In making this decision, the FDA conceded it ...
