The U.S. Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services and is responsible for the safety regulation of most types of foods, dietary supplements, drugs, vaccines, biological medical products, blood products, medical devices, radiation-emitting devices, veterinary products, and cosmetics. The FDA also enforces section 361 of the Public Health Service Act and the associated regulations, including sanitation requirements on interstate travel as well as specific rules for control of disease on products ranging from pet turtles to semen donations for assisted reproductive medicine techniques. Read more at Wikipedia


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...reconfirmed all previous late-stage study results. This data is strong enough for AcelRx to seek approval from the Food and Drug Administration with a new drug application filing expected next quarter. I'd be cautious with AcelRx moving forward, as the possibility...

FORUM: Sexual double standard denies girls access to protection

...also that adolescents understand it is not for routine use and doesn’t protect against sexually transmitted diseases. Food and Drug Administration Commissioner Margaret Hamburg, who is a physician, concluded that “there is adequate and reasonable, well-supported,...

Kalamazoo march against Monsanto, GMO foods draws hundreds

...undergo detailed scientific review by at least two, and often three separate federal agencies, including the U.S. Food and Drug Administration; the Environmental Protection Agency and the U.S. Department of Agriculture.” Helscher said biotechnology crops require...

Waterville nursing home pioneer in treatment of dementia patients

...health care leaders have been working to prevent the overmedication of seniors since 2005, when a report from the Food and Drug Administration showed they may have a lower quality of life and even die from some antipsychotic medications, which can cause heart...

Read labels make judicious sunscreen choices

...rays, SPF 100 provides you with 99 per cent protection (some experts even say that it is only 98 per cent). In fact, the Food and Drug Administration (FDA) in the United States says there is no sufficient data to show that products with values higher than...

Tough rules for US manufactured foods

...“Research shows people want to have the nutrition information. They make better choices when they have the numbers.” The Food and Drug Administration hopes to have the regulations in place later this year. Restaurants would likely have six months from then...

Protesters push for labeling of genetically modified foods

...genetically modified products even though the federal government and many scientists say the technology is safe. The Food and Drug Administration does not require the labeling, but organic food companies and some consumer groups have intensified their push...

Lipsonix could provide a solution for obesity: clinic

...control their diets. The clinic noted that Liposonix â which is approved by Taiwan's Department of Health and the U.S. Food and Drug Administration â may provide a solution to the problem. Liposonix is a nonsurgical and noninvasive treatment that uses high-intensity...

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FDA Looking at Caffeinated Foods and Their Negative Effects on Kids

The Food and Drug Administration is taking a fresh look at caffeinated products now that the stimulant is being added to all types of food. Caffeine can be found in everything from jelly beans to waffles, and most recently, gum.

Drug Safety and Approval Is About Trusting Government

The Food and Drug Administration, the oldest comprehensive consumer protection agency in the U.S. federal government, is charged with protecting the public health. Under this mandate, it regulates drugs and medical devices for their safety and effectiveness. But is it a failing mandate?

Peter Huber on How FDA Bureaucracy Holds Back Science

The Food and Drug Administration, the oldest comprehensive consumer protection agency in the U.S. federal government, is charged with protecting the public health. Under this mandate, it regulates drugs and medical devices for their safety and effectiveness. But is it a failing mandate? It's long been argued that the FDA's long and costly approval processes stifle innovation.

Whole Foods Mixes Up Chicken and Vegan Salad Labels

Whole Foods Market says the labels on a curried chicken salad were switched with those on a vegan version of the salad at 15 stores throughout the Northeast. The grocer says the mislabeled salads came from a third-party vendor. No one has reported getting sick, but Patrick Jones says, the Food and Drug Administration notes the mistake could have ended worse.

FDA Investigating Caffeinated Gum

Wrigley says it is taking a new caffeinated gum off the market temporarily as the Food and Drug Administration investigates the safety of added caffeine.

FDA Approves Lower Age For Morning After Pill

Tuesday the U.S. Food and Drug Administration announced approval for over-the-counter sales of Plan B One-Step to women 15 years of age and older. The amended application was submitted to the F.D.A. for approval by Teva Women’s Health, Inc. The F.D.A.’s decision will make the product available to women 15 years of age and older without a prescription or parental consent.

Obama: I'm "Comfortable" With FDA Decision To Sell Morning-After Pill To 15 Year Olds

President Obama on Thursday told reporters he is "comfortable" with a Food and Drug Administration decision to allow girls 15 years of age and older to buy the morning-after pill (Plan B) over the counter. "I'm very comfortable with the decision they've made right now based on solid scientific evidence for girls 15 and older," President Obama said at a press conference in Mexico City with Mexican President Pena Nieto. "I'm very comfortable with contraception," Obama told reporters. "I think it is very important that women have control over their healthcare choices and when they are starting a family. That is their decision to make. And so we want to make sure they have access to contraception. As you know, we have a little bit of a fuss around what we're doing with the Affordable Care Act. But I very much think that is the right thing to do."

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The U.S. Department of Health and Human Services building which houses the Food and Drug Administration (FDA) in Rockville, MD. (Getty Images) - Published on 2013-05-24 16:43:00 by WOAI

The U.S. Department of Health and Human Services building which houses the Food and Drug Administration (FDA) in Rockville, MD. (Getty Images)

Published by WOAI on 2013-05-24 16:43:00

The U.S. Department of Health and Human Services building which houses the Food and Drug Administration (FDA) in Rockville, MD. (Getty Images) - Published on 2013-05-24 16:43:00 by 13WHAM-TV

The U.S. Department of Health and Human Services building which houses the Food and Drug Administration (FDA) in Rockville, MD. (Getty Images)

Published by 13WHAM-TV on 2013-05-24 16:43:00

Jane Michalek (R) drinks soup during an eat-in protest in front of the U.S. Food and Drug Administration's Center for Food Safety and Applied Nutrition in College Park, Maryland (Reuters / Gary Cameron) - Published on 2013-05-24 05:51:00 by Russia Today

Jane Michalek (R) drinks soup during an eat-in protest in front of the U.S. Food and Drug Administration's Center for Food Safety and Applied Nutrition in College Park, Maryland (Reuters / Gary Cameron)

Published by Russia Today on 2013-05-24 05:51:00

The US Food and Drug Administration imposed an 'import alert' on a plant operated by the generic drugmaker. - Published on 2013-05-24 01:23:00 by Economic Times

The US Food and Drug Administration imposed an 'import alert' on a plant operated by the generic drugmaker.

Published by Economic Times on 2013-05-24 01:23:00

The U.S. Food and Drug Administration says despite studies suggesting the contrary, heartburn drugs Nexium and Prilosec do not increase the risk of heart problems. (ABCNEWS) - Published on 2013-05-23 17:07:00 by WLS

The U.S. Food and Drug Administration says despite studies suggesting the contrary, heartburn drugs Nexium and Prilosec do not increase the risk of heart problems. (ABCNEWS)

Published by WLS on 2013-05-23 17:07:00

Wockhardt Ltd said up to $100 million in annualised revenue could be lost as a result of a US Food and Drug Administration 'import alert' on one of its plants. - Published on 2013-05-23 08:13:00 by Economic Times

Wockhardt Ltd said up to $100 million in annualised revenue could be lost as a result of a US Food and Drug Administration 'import alert' on one of its plants.

Published by Economic Times on 2013-05-23 08:13:00


Algeta’s drug, Xofigo, (radium-223 dichloride), an injection for the treatment of patients with castration-resistant prostate cancer, symptomatic bone metastases and no known visceral metastatic disease, was approved by the U.S. Food and Drug Administration.


 - Published on 2013-05-15 12:16:00 by Boston Business Journal

Algeta’s drug, Xofigo, (radium-223 dichloride), an injection for the treatment of patients with castration-resistant prostate cancer, symptomatic bone metastases and no known visceral metastatic disease, was approved by the U.S. Food and Drug Administration.

Published by Boston Business Journal on 2013-05-15 12:16:00

Jane Michalek (R) drinks soup during an eat-in protest in front of the U.S. Food and Drug Administration's Center for Food Safety and Applied Nutrition in College Park, Maryland April 8, 2013. (Reuters) - Published on 2013-05-14 16:38:00 by Russia Today

Jane Michalek (R) drinks soup during an eat-in protest in front of the U.S. Food and Drug Administration's Center for Food Safety and Applied Nutrition in College Park, Maryland April 8, 2013. (Reuters)

Published by Russia Today on 2013-05-14 16:38:00

Ohio Attorney General Mike DeWine on Monday asked the U.S. Food and Drug Administration (FDA) to begin labeling addictive prescription painkillers with warnings for expectant mothers. - Published on 2013-05-14 07:41:00 by Dayton Business Journal

Ohio Attorney General Mike DeWine on Monday asked the U.S. Food and Drug Administration (FDA) to begin labeling addictive prescription painkillers with warnings for expectant mothers.

Published by Dayton Business Journal on 2013-05-14 07:41:00

The  Plan B One-Step (levonorgestrel) is one of the brands known as the

The Plan B One-Step (levonorgestrel) is one of the brands known as the "morning-after pill." The Plan B morning-after pill is moving over-the-counter, a decision announced by the Food and Drug Administration just days before a court-imposed deadline.

Published by New York Daily News on 2013-05-13 12:57:00

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North Carolina authorities said skin abscesses have been the complications identified so far...

in Tennessee Pharmacy Steroid Injections Recalled After Complications Arise
RedOrbit - 2013-05-25 06:08:00

When these dipsticks are read by an automated strip reader, the dipsticks require new clearance as part of the test system ... Therefore, any company intending to promote their device for use in analyzing, reading, and/or interpreting these dipsticks needs to obtain clearance for the entire urinalysis test system (i.e., the strip reader and the test strips, as used together)....

in FDA says maker of urine analysis app needs federal approval
iStockAnalyst - 2013-05-25 04:43:00

This can’t be a field of dreams, where if we grow it this way, they will buy it no matter the cost...

in On the Front Lines of Food Safety
The New York Times - 2013-05-24 23:55:00

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