Top 97 Fda Quotes & Sayings

Explore popular Fda quotes.
Last updated on December 21, 2024.
For the first time since 2007, the FDA Has approved a new device to treat obesity. The amazing breakthrough is called a vegetable.
The people who work at FDA are just trying to do their jobs.
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.
Unfortunately, beer was only a short-term answer. And head transplants had yet to be approved by the FDA. — © J.R. Ward
Unfortunately, beer was only a short-term answer. And head transplants had yet to be approved by the FDA.
I think FDA's concerns are patient-safety.
The FDA is redefining birth control as abortion. The FDA is setting the bar higher for this kind of drug.
The food industry, its trade associations, and research foundations, is well financed and highly organized to pressure the FDA.
People think the FDA is protecting them -- it isn't. What the FDA is doing, and what people think it's doing, are as different as night and day.
As was noted in the Wall Street Journal, last March 21st, FDA approval of drug labelling, '...requires seven to ten years, and costs each applicant an average of $70 million.'
If you go to the FDA with a drug that's only meant to treat 50 people, and it's a 95 percent cure rate, you'll get your drug approved.
It's a terrible thing that we cannot really trust the FDA or NCI (National Cancer Institute). We need, therefore, an independent scientific investigation.
First, it is providing a means whereby key individuals on its payroll are able to obtain both power and wealth through granting special favors to certain politically influential groups that are subject to its regulation. This activity is similar to the 'protection racket' of organized crime: for a price, one can induce FDA administrators to provide 'protection' from the FDA itself.
We have the opportunity to provide the first FDA reviewed and approved over-the-counter option that can help people lose weight and make changes to their lifestyle and diet.
I have smuggled so many ingredients across so many borders, like shallot confit from Thailand, or a new sauce from New Orleans not approved by the FDA.
And thirdly, the FDA occasionally does some genuine public good with whatever energies it has left over after serving the vested political and commercial interest of its first two activities.
To speak only of food inspections: the United States currently imports 80% of its seafood, 32% of its fruits and nuts, 13% of its vegetables, and 10% of its meats. In 2007, these foods arrived in 25,000 shipments a day from about 100 countries. The FDA was able to inspect about 1% of these shipments, down from 8% in 1992. In contrast, the USDA is able to inspect 16% of the foods under its purview. By one assessment, the FDA has become so short-staffed that it would take the agency 1,900 years to inspect every foreign plant that exports food to the United States.
The public properly relies upon FDA classification of drugs as nonprescription as a reflection of the agency's judgment regarding the safety and proper use of a drug without a doctor's prescription.
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.
It's unfortunate, and we're disappointed the FDA did not grant the stay, ... But because there are no new scientific findings other than what the poultry groups submitted already, the likelihood of the company being successful in a further legal action is next to nil.
I think that the FDA has not been able to catch some of these things as quickly as I expect them to catch and so we’re going to be doing a complete review of FDA operations. At bare minimum, we should be able to count on our government keeping our kids safe when they eat peanut butter. That’s what Sasha eats for lunch. Probably three times a week...
I have had a long tug-of-war going on with the FDA, in particular, and with other regulatory agencies, and it has nothing to do with vaccines. — © Jill Stein
I have had a long tug-of-war going on with the FDA, in particular, and with other regulatory agencies, and it has nothing to do with vaccines.
I'm offering solutions to address rising healthcare prices by adding transparency to our drug pricing, clearing the backlog on pending drug applications at the FDA, and providing oversight and accountability within the healthcare industry.
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.
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.
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.
Some of the FDA's own scientists have charged that politics, not science, is behind the FDA's actions.
FDA clearance is an important step on the path towards getting genetic information integrated with routine medical care.
My struggles have been around protecting our air quality, protecting people from mercury in fish. I was very involved in the effort to get the FDA to recognize that mercury in fish is a real health issue and the FDA, you know, needed to be on that. But they were very tight with the fishing industry and did not want the public to be aware in the same way that they later didn't want the public to be aware of the problems with Vioxx, and they sat on the studies for many years and allowed 140,000 people to develop heart disease.
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.
Patients who face long odds and terminal illnesses do not always have access to the latest drugs in clinical trials. They don't want to give up, but they don't have years to wait for new drugs to receive FDA approval.
The FDA has formed a rapid response team.
The FDA serves a real purpose: To protect public health.
There is a nationwide shortage of drugs for Attention Deficit Disorder. The FDA says they're not sure how it happened. I guess somebody wasn't paying attention.
Coke and Pepsi, with the acquiescence of the FDA, are needlessly exposing millions of Americans to a chemical that causes cancer.
It's time to get the FDA to reverse its 1994 decision not to label GM foods.
By giving the FDA adequate resources and authority to both prevent outbreaks and intervene once they appear, we can support the administration's efforts to reassure the parents of America that the food they feed their children is the product of the safest system in the world.
Policies I advanced as FDA commissioner aimed to get smokers off cigarettes and onto less-harmful forms of nicotine delivery.
A lot of great medicines and ancient therapies are blocked by the FDA, so that's why I choose to travel and recognize the value of diverse points of view in medicine.
When the FDA announced its intentions to join other countries and ban quinolone use on U.S. chicken farms, the drug manufacturer Bayer initiated legal action that successfully delayed the process for five years.
However, FDA attempted to reverse this clear congressional intent in March, 1979, by proposing to regulate vitamins and minerals as 'Over-The-Counter' drugs. — © Orrin Hatch
However, FDA attempted to reverse this clear congressional intent in March, 1979, by proposing to regulate vitamins and minerals as 'Over-The-Counter' drugs.
While faulty information from a digital health tool can influence people to make bad decisions, the risks are far lower than those posed by the usual products FDA subjects to pre-market review.
If music ever needs FDA approval in the future, bands like this will be the reason why; Magic Kids' sugar-coated songs paint a mental picture of smiling clouds and double rainbows, with a unicorn or two tossed in for good measure.
Secondly, as a result of this political favoritism, the FDA has become a primary factor in that formula whereby cartel-oriented companies in the food and drug industry are able to use the police powers of government to harass or destroy their free-market competitors.
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.
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
I've heard drug experts say they believe if penicillin were discovered today, the FDA wouldn't license it.
The FDA has received over a million comments from citizens demanding labeling of GMOs. 90 percent of Americans agree. So, why no labeling?
If you're trying to develop a new drug, that costs you a billion dollars to get through the FDA. If you want to start a software company, you can get started with maybe $100,000.
22 of 52 top (FDA) officials have worked for regulated industries, or organizations that cater to those industries...During a hearing held in 1969 by the House Inter-governmental Relations Subcommittee, it was disclosed that of 49 high ranking FDA officials who had recently resigned or retired, 37 joined or served as consultants to regulated industries.
The FDA is now warning people not to eat raw cookie dough this holiday season. Is that how fat we're getting in this country? Our ovens are too slow now?
Increasing patient access to more affordable, FDA-approved generic and biosimilar medicines is a proven and tested solution to lowering prescription drug costs.
They're putting cement dust into cattle feed to make the cows heavier; the FDA knows all about it.
Being the first FDA-authorized direct-to-consumer genetic test out there is revolutionary.
The FDA and much, but not all, of the orthodox medical profession are actively hostile against vitamins and minerals... They are out to get the health food industry...And they are trying to do this out of active hostility and prejudice.
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.
You may have difficulty in obtaining some of these (non-drug) therapies..because the FDA has literally pressured Congress, under the guise of protecting the public, to keep time-honoured cultural and natural therapies out of the hands of the general public. If you look at the record of the FDA, it becomes obvious they are serving interests other than yours and mine.
If a State has reliable scientific information that demonstrates that a warning is needed for a particular food, then in the interest of public health, it should share that information with the FDA and petition for a new national standard.
My manager says we've been working with the FDA on this. — © Carlos Gonzalez
My manager says we've been working with the FDA on this.
Gifted Nutrition was able to show me that they had FDA-compliant ingredients in their supplements. I thought that was really huge, especially when you are trying to show people that you are a natural athlete.
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