Sentences with phrase «federal food and drug»

(T) an oral drug (which is approved by the federal Food and Drug Administration) prescribed for use as an acute anti-emetic used as part of an anti-cancer chemotherapeutic regimen * * *

He focuses his practice on federal Food and Drug Administration (FDA) regulatory matters.

The federal Food and Drug Administration warns that raw, or unpasteurized, milk can contain harmful bacteria, and Maryland law prohibits its sale.

Defective Medical Products The Federal Food and Drug administration is the agency in charge of monitoring medical devices in this country.

Even when a drug has been approved by the federal Food and Drug Administration, it sometimes turns out to be unsafe for long - term use and causes more harm than good, such as a popular weight loss drug that caused serious health problems in many of its users and was pulled from the market.

In light of a recent safety announcement by the federal Food and Drug Administration, U.S. regulators are reviewing the safety of the diabetes medication, Avandia, which is made by GlaxoSmithKline.

In Arizona, Nebraska, and Texas, efforts to import execution drugs from India have been stymied by the federal Food and Drug Administration.

The federal Food and Drug Administration's (FDA) Center for Veterinary Medicine is investigating deaths and

According to NBC News, «Federal Food and Drug Administration officials unexpectedly posted summaries this week of lab results of nearly 300 jerky treat samples collected and tested in the U.S. between April 2007 and June 2012.»

The pace of the reported illnesses appears to have slowed, but federal Food and Drug Administration officials are now seeking extra help from veterinarians and pet owners in solving the ongoing puzzle.

(3) All New Mexico board of pharmacy, New Mexico Controlled Substances Act, federal drug enforcement administration (DEA) and federal food and drug administration requirements shall be complied with, including but not limited to the following:

The federal Food and Drug Administration's (FDA) Center for Veterinary Medicine is investigating deaths and illnesses resulting from chicken, duck and sweet potato jerky treats made in China.

The centralized model of investing in research may work in medicine, where the federal Food and Drug Administration must approve drugs and where there is a vast network of medical journals and professional societies for disseminating the latest findings.

However, the federal Food and Drug Administration has not approved its use for children under the age of 6.

These toxic and dangerous drugs are kept legal by the federal Food and Drug Administration (FDA) which actively suppresses any competing natural cure that has no dangerous side effects.

``... Custom - compounded hormones are not approved by the federal Food and Drug Administration and have not been proved safe or effective.

The bill would also allow foods labeled as «natural» to contain GE foods, and prevent the federal Food and Drug Administration from requiring mandatory labeling.

A bill introduced by Sens. Dianne Feinstein, D - Calif., and Susan Collins, R - Maine, would help the federal Food and Drug Administration ensure that...

Horseshoe crab blood carries a clotting agent that can isolate bacterial toxins — and the federal Food and Drug Administration requires that it be used to test all intravenous drugs and vaccines for safety.

The authors expect the federal Food and Drug Administration (FDA) will approve at least one gene therapy treatment within the next three years.

BPA is no longer used in baby bottles and sippy cups in the United States, but the federal Food and Drug Administration has maintained the levels that may leach from canned goods into food do not pose a risk to human health.

Many patients and physicians assume that the safety and effectiveness of newly approved drugs is well understood by the federal Food and Drug Administration (FDA)-- but a new study by researchers at Yale School of Medicine shows that the clinical trials used by the FDA to approve new drugs between 2005 and 2012 vary widely in their thoroughness.

Researchers estimate that as many as 2.1 million patients with mild cognitive impairment could develop Alzheimer's dementia over a two - decade period while waiting for evaluation and treatment resources after approval of an Alzheimer's disease - modifying therapy by the federal Food and Drug Administration.

The team is conducting additional research toward an investigational new drug application from the federal Food and Drug Admission.

Researchers say the results provide information that the federal Food and Drug Administration's Center for Tobacco Products could potentially use to make future regulatory decisions for point - of - sale tobacco advertising.

Some lawmakers were concerned about a potential tax reduction for «reduced harm tobacco products» that have not been approved by the federal Food and Drug Administration and are not yet on the market.

Of the 22 homes, four tested above the federal Food and Drug Administration's standard for lead in bottled water.

And just this month, the federal Food and Drug Administration requested Endo Pharmaceuticals, an international pharmaceutical manufacturer, remove Opana ER — a semi-synthetic opioid painkiller — from the market after concluding the drug's potential for abuse outweighed its therapeutic value.

ESD chief operating officer Kevin Younis said the decision about Athenex was made because of its experience dealing with the federal Food and Drug Administration, and was not a sign of a blanket policy shift.

Senator Phil Boyle, a Long Island Republican, said the bill was necessary because the federal Food and Drug Administration was not moving quickly enough to regulate chemicals that could harm children.

The federal Food and Drug Administration (FDA) has approved the addition of two long - chain fatty acids to formula: DHA (docosahexaenoic acid) and ARA (arachidonic acid), which are now standard ingredients in formula.

Nearly 207 million eggs from a farm in North Carolina are being recalled from nine U.S. states after 22 people fell ill, the federal Food and Drug Administration has said.

April 15 - Nearly 207 million eggs from a farm in North Carolina are being recalled from nine U.S. states after 22 people fell ill, the federal Food and Drug Administration has said.

A government agency established in 1906 with the passage of the Federal Food and Drugs Act.

Under the Federal Food and Drugs Act, it's illegal to ship a drug across state lines that hasn't been approved by the U.S. Food and Drug Administration (FDA) for human use.

Not exact matches

In the FDA's warning letter this week, the agency excoriated Meridian for what it had found, laying out «significant violations» of the Federal Food, Drug and Cosmetic Act.

According to the Federal Food, Drug, and Cosmetic Act, the FDA can only require foods to be labeled as GMO if there is a material difference between the GM product and its non-GM counterpart.

The U.S. Food and Drug Administration and the Federal Trade Commission issued 13 letters to manufacturers, distributors and retailers, saying the packaging resembles kid - friendly food products sucFood and Drug Administration and the Federal Trade Commission issued 13 letters to manufacturers, distributors and retailers, saying the packaging resembles kid - friendly food products sucfood products such...

The packaging resembles that of juice boxes, candy or cookies, the U.S. Food and Drug Administration and the Federal Trade Commission said, noting a recent increase in the number of reports to poison control centers.

The rare pediatric disease priority review voucher program under section 529 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360ff).

U.S. Food and Drug Administration chief Scott Gottlieb on Thursday questioned whether rebates that drugmakers provide to health insurers should remain protected by federal law, sparking new concerns on Wall Street over efforts to curb drug pricDrug Administration chief Scott Gottlieb on Thursday questioned whether rebates that drugmakers provide to health insurers should remain protected by federal law, sparking new concerns on Wall Street over efforts to curb drug pricdrug pricing.

A federal appeals court ruled in 2015 that the notice can't take place until after biosimilar makers gain approval from the Food and Drug Administration.

An Abbreviated New Drug Submission (ANDS) must be approved by Health Canada, the country's federal department in charge of national health care, under Canada's Food and Drug regulations before the generic drug can be marketed in the counDrug Submission (ANDS) must be approved by Health Canada, the country's federal department in charge of national health care, under Canada's Food and Drug regulations before the generic drug can be marketed in the counDrug regulations before the generic drug can be marketed in the coundrug can be marketed in the country.

(e) If test results indicate a specific agricultural product contains pesticide residues or environmental contaminants that exceed the Food and Drug Administration's or the Environmental Protection Agency's regulatory tolerences, the certifying agent must promptly report such data to the Federal health agency whose regulatory tolerance or action level has been exceeded.

Although many of these claims challenge the veracity of «organic,» «healthy,» and «100 %» claims on labels, several states are affording new opportunities to attack ingredient labels — an area that federal courts have traditionally found to be preempted (barred) by the Food and Drug Administration (FDA) with no private right of action for individual citizens.

The Nutrition Labeling and Education Act (NLEA), which amended the Federal Food, Drug, and Cosmetic Act (FDCA) to give the FDA authority to require nutrition labeling on virtually all food products, provides no private right of action for individuals to enforce the provisions of the NFood, Drug, and Cosmetic Act (FDCA) to give the FDA authority to require nutrition labeling on virtually all food products, provides no private right of action for individuals to enforce the provisions of the Nfood products, provides no private right of action for individuals to enforce the provisions of the NLEA.

The United States Department of Agriculture (USDA) and the Food and Drug Administration (FDA) are the two federal agencies in the United States responsible for protecting consumer rights in regards to food safFood and Drug Administration (FDA) are the two federal agencies in the United States responsible for protecting consumer rights in regards to food saffood safety.

The United States Department of Agriculture (USDA) and the U.S. Food and Drug Administration (FDA) are the two federal agencies in the United States responsible for protecting consumer rights in regards to food safFood and Drug Administration (FDA) are the two federal agencies in the United States responsible for protecting consumer rights in regards to food saffood safety.

* The statements on this page have not been evaluated by the Food and Drug Administration (FDA) or the Federal Trade Commission (FTC).

Last year, after the Food and Drug Administration and Federal Trade Commission told the four biggest manufacturers of alcoholic energy drinks the caffeine in their beverages was... Continue Reading