A Quote by Dean Burk

Such letters...from the FDA, are, filled with objectively demonstrable lies, practiced deceptions and deviousness, red herrings, directed misinformation, misdirected information, etc. ...Once FDA-NCI-AMA-ACS...concedes that Laetrile anti-tumor efficacy was indeed even once observed...a permanent crack in bureaucratic armor has taken place.
When the FDA forces an old drug off the market, patients have very little say in the matter. Patients have even less of a say when the FDA chooses not to approve a new drug. Instead, we are supposed to rely on the FDA's judgment and be grateful. But can the FDA really make a choice that is appropriate for everyone? Of course not.
If these restrictions were necessary, the FDA would have promulgated them in the first place, the FDA knows how to evaluate scientific information. Congress knows nothing about that.
You wouldn't believe how many FDA officials or relatives or acquaintances of FDA officials come to see me as patients in Hanover. You wouldn't believe this, or directors of the AMA, or ACA, or the presidents of orthodox cancer institutes. That's the fact
Dean Burk, PhD, of the National Cancer Institute (head of their Cytochemistry Section and 32-year veteran at the agency) declared in a (May 30,1972) letter to (congressman Louis Frey, Jr.) that high officials of the FDA, AMA and ACS (American Cancer Society), were deliberately falsifying information, literally lying...and in other ways thwarting potential cancer cures to which they were opposed.
The field of U.S. cancer care is organized around a medical monopoly that ensures a continuous flow of money to the pharmaceutical companies, medical technology firms, research institutes, and government agencies such as the Food and Drug Administration (FDA) and the National Cancer Institute (NCI) and quasi-public organizations such as the American Cancer Society (ACS).
Some of the FDA's own scientists have charged that politics, not science, is behind the FDA's actions.
The FDA is redefining birth control as abortion. The FDA is setting the bar higher for this kind of drug.
The (Laetrile) efficacy tests...clinically in humans..(by) the US NCI...were obviously conducted so that a negative result could be formulated. The limited number and types of human cancer cases selected...the omission of necessary additional measures ('e.g dietary'), the far too short observation periods, and the undefined chemical properties of the (Laetrile)... all contributed to devaluation of...conclusions.
It's a terrible thing that we cannot really trust the FDA or NCI (National Cancer Institute). We need, therefore, an independent scientific investigation.
The thing that bugs me is that the people think the FDA is protecting them - it isn’t. What the FDA is doing and what the public thinks it’s doing are as different as night and day.
It disturbs me mostly...is the willful, deliberate denial (by the FDA, of) our own citizens, a fair chance to use Laetrile, when all the record (shows) it is not toxic, ... is safe, ... and is effective.
By law and institutional culture, FDA seeks to apply a single tool to its approach to regulation - the requirement for pre-market approval. The agency is accustomed to compelling innovators to submit evidence to FDA and seek permission for marketing.
The FDA, NCI and ACS, and the large treatment centres work to eliminate choice of cancer therapies, particulary better ones. They openly attack breakthroughs made by "mavericks", which they define as anyone outside their ranks. Folks, any serious study of how these entities work together to destroy hopeful approaches to cancer reveals a trail of corruption, conspiracy, dishonesty, and inhumanity that warrants desigantion of evil........We continue to use them not because they work, but because those who perform them have so vigorously eliminated any other choice.
Remember, FDA employees are serious about fear. We pay these people to panic about an iota of rodent hair in our chili, even when the recipe calls for it. FDA employees are first-class agonizers, world champions at losing sleep. When Meryl Streep got hysterical about Alar, they actually checked the apples instead of Meryl's head.
Food safety oversight is largely, but not exclusively, divided between two agencies, the FDA and the USDA. The USDA mostly oversees meat and poultry; the FDA mostly handles everything else, including pet food and animal feed. Although this division of responsibility means that the FDA is responsible for 80% of the food supply, it only gets 20% of the federal budget for this purpose. In contrast, the USDA gets 80% of the budget for 20% of the foods. This uneven distribution is the result of a little history and a lot of politics.
I think every doctor should know the shocking state of affairs...We discovered they (the FDA) failed to effectively regulate the large manufacturers and powerful interests while recklessly persecuting the small manufacturers. ...(The FDA is) harassing (small) manufacturers and doctors...(and) betrays the public trust.
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