FDA的意思|FDA的解释-里氏词典

FDA

abbr. Food and Drug Administration(美国)食品及药物管理局

fda

[ noun ]
a federal agency in the Department of Health and Human Services established to regulate the release of new foods and health-related products
<noun.group>

Last year, the FDA said it would allow people with life-threatening illnesses to import personal supplies of unapproved drugs.
Mossinghoff acknowledged that "a subliminal purpose (for the press conference) is to let elder Americans know that it is important for the FDA to have adequate funding" to review these new drugs.
He is prepared to spend his money in the U.S. instead if the new FDA rules make the drugs available here.
Meanwhile, the FDA conducted tests on the different fruits to identify the detectable damage caused by cyanide injections, so inspectors would know what to look for.
The company's stock, which had traded as high as $22.50 during the past year, slid to $13 after the FDA hearing and closed yesterday at $8.75, down 50 cents, in national over-the-counter trading.
National Gay Rights Advocates, a California public interest law firm, has filed a class action suit on behalf of AIDS patients against the Department of Health and Human Services, FDA and National Institutes of Health.
Sullivan assured panel members that he is putting the FDA's house in order, restructuring its management and adding resources in the wake of the generic drug fraud and corruption scandal.
They're afraid that the FDA's bureaucrats, many of whom are fighting the proposal, will drag their feet in giving formal approval for drugs being distributed to patients under the new rules.
The public controversy over bST is unusual because the FDA does not normally discuss the merits of products before they are approved.
Without the "strongest action" from FDA to stop the misleading claims, "we are approaching total chaos in the marketplace," Weiss said.
There's talk now that the FDA is pondering making implants available only to women who have lost breasts to cancer.
It is unclear what importance the FDA attached to such evidence during Dr. Cooper's tenure.
But the FDA's letter to P&G says the product is a new drug, regardless of specific claims about the product.
Over the years, the FDA has granted dozens of extensions to allow Red No. 3 to remain on the provisional list.
The subcommittee also said it has "preliminary information" that two other generic drug makers "may have made misrepresentations" to obtain FDA clearance for diazepam, the generic version of Valium, also used for epilepsy.
Recommendations are expected within 45 days. Saline-filled implants will not be affected by the moratorium. According to the FDA, about 20 per cent of the 1m women in the US with implants have them for breast reconstruction after cancer surgery.
The FDA said it is working with state authorities and the U.S. Customs Service, Postal Service and the Federal Trade Commission to curb the proliferation of illegal versions of Retin-A.
Such testing can take six months to two years or longer, and the FDA's ruling effectively killed Favor.
The FDA meets regularly with drug companies testing new drugs to advise the companies on what further research is needed for approval.
Now the FDA has invoked essentially the same procedure that would be used to establish the safety of a new product, but has no standing to remove breast implants from the market in the absence of clear evidence that they are a definite health risk.
Bristol-Myers blamed bureaucratic sluggishness at the FDA for the delay.
In a ruling from the bench Tuesday, Judge Marshall rejected the FDA's position and reissued his order requiring the doctors' names to go to the plaintiffs' lawyers.
The Justice Department is investigating an American Cyanamid employee, believed to have altered the research results, and the FDA is exploring if Cyanamid's management knew of any data falsification.
The FDA is expected to take months to settle on a way to test claims about a product's ability to degrade.
Brad Stone, an FDA spokesman, said the agency is encouraged by the Red Cross' latest moves _ particularly the trend to centralize operations.
The amendment said it isn't patent infringement to use or sell a "patented invention" of another company if the purpose is "reasonably related" to obtaining data to submit to the FDA.
Another gene-therapy experiment, also approved by NIH last week and awaiting FDA clearance, would treat patients with a lethal form of skin cancer.
The FDA's regulatory timetable is mandated by the Nutrition Labeling and Education Act of 1990.
The FDA has banned the drug for dairy cattle, and plans to propose a further ban for beef cattle and pigs.
Abbott Laboratories won FDA approval of its new estazolam insomnia drug, which will compete against Upjohn's Halcion. Separately, Johnson & Johnson won approval to sell its brand of a big-selling anemia drug.

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