Sentences with phrase «drug administration today»

The U.S. Food and Drug Administration today approved lorcaserin hydrochloride as a weight - loss drug, according to MedPage Today.

The U.S. Food and Drug Administration today approved Tresiba (insulin degludec injection) and Ryzodeg 70/30 (insulin degludec / insulin aspart injection) to improve blood sugar (glucose) control in adults with diabetes mellitus.

The vexing problem is not going away, but the U.S. Food and Drug Administration today rolled out new plans designed to help stymie the shortages.

The U.S. Food and Drug Administration today approved a new immunotherapy drug to treat advanced melanoma, signaling a paradigm shift in the way the deadly skin cancer is treated.

The U.S. Food and Drug Administration today proposed two new food safety rules that will help prevent foodborne illness.

Not exact matches

SAN JOSE, Calif., April 25, 2018 (GLOBE NEWSWIRE)-- Align Technology, Inc. (NASDAQ: ALGN) today announced that the company has received approval from the China Food and Drug Administration (CFDA) to market the iTero Element intraoral scanner in China.

«Our policies from the last Administration — and quite frankly the Democrat policies of today — of an open border and sanctuary cities allow and enables these drug smugglers who don't care about human life to put people in this horrific situation,» Patrick said.

An expert panel for the U.S. Food and Drug Administration voted today to approve a drug that has been dubbed the «female Viagra» after two previous attempts failed to gain approDrug Administration voted today to approve a drug that has been dubbed the «female Viagra» after two previous attempts failed to gain approdrug that has been dubbed the «female Viagra» after two previous attempts failed to gain approval.

Cambridge, MA — February 6, 2017 — Aura Biosciences, a biotechnology company developing a new class of therapies to target and selectively destroy cancer cells using viral nanoparticle conjugates, announced today that the U.S. Food and Drug Administration (FDA) has cleared the investigational new drug application (IND) for the company's lead program, light - activated AU - 011 in ocular melanoma (Drug Administration (FDA) has cleared the investigational new drug application (IND) for the company's lead program, light - activated AU - 011 in ocular melanoma (drug application (IND) for the company's lead program, light - activated AU - 011 in ocular melanoma (OM).

Aura additionally announced today that the U.S. Food and Drug Administration (FDA) has granted AU - 011 fast track designation for the treatment of primary ocular melanoma, also known as uveal or choroidal melanoma.

WASHINGTON, D.C. - The Grocery Manufacturers Association (GMA) today urged President Bush to call for increased funding for the Food and Drug Administration (FDA) during tonight's State of the Union Address to the nation.

Grocery Manufacturers Association (GMA) Executive Vice President of Policy and Strategic Planning Mary Sophos delivered today's keynote address at the Food and Drug Administration's (FDA) public meeting on international food safety capacity building as it relates to the Food Safety Modernization Act (FSMA).

(WASHINGTON, D.C.) The Grocery Manufacturers Association (GMA) today welcomed the Food and Drug Administration's (FDA) proposed extension of the compliance date for label changes to the Nutrition Facts Panel (NFP) on food and beverage products to January 1, 2020.

(Washington, D.C.) The Grocery Manufacturers Association (GMA) today issued the following statement in response to the Food and Drug Administration's Notice of Final Determination on Generally Recognized as Safe (GRAS) status of Partially Hydrogenated Oils (PHOs):

The Grocery Manufacturers Association issued the following statement by Leon Bruner, Chief Science Officer, on the draft sodium reduction guidelines and food category targets released today by the U.S. Food and Drug Administration (FDA).

Today, the Glass Packaging Institute (GPI) announced its concern over the U.S. Food and Drug Administration's (FDA) decision rejecting a call to ban the use of bisphenol A (BPA) in food packaging in even the most vulnerable populations such as children and child - bearing women.

Glass Packaging Institute Expresses Concern over FDA Decision on BPA, March 30, 2012 Today, the Glass Packaging Institute (GPI) announced its concern over the U.S. Food and Drug Administration's (FDA) decision rejecting a call to ban the use of bisphenol A (BPA) in food packaging in even the most vulnerable populations such as children and child - bearing women.

(WASHINGTON, D.C.) The Grocery Manufacturers Association (GMA) today applauded the Food and Drug Administration (FDA) announced intention to extend the compliance date for label changes to the Nutrition Facts Panel (NFP) on food and beverage products.

The Grocery Manufacturers Association today issued the following statement by Pamela G. Bailey, president and CEO, on the announcement that President - elect Trump intends to nominate Scott Gottlieb as Commissioner of the Food and Drug Administration.

ALEXANDRIA, Va., — Today, the Glass Packaging Institute (GPI) announced its concern over the U.S. Food and Drug Administration's (FDA) decision rejecting a call to ban the use of bisphenol A (BPA) in food packaging in even the most vulnerable populations such as children and child - bearing women.

(Washington, D.C.) The Grocery Manufacturers Association (GMA) issued the following statement from Dr. Leon Bruner, GMA's chief science officer, on the release today of a newNutrition Facts panel by the U.S. Food and Drug Administration (FDA):

The Grocery Manufacturers Association (GMA) issued the following statement from Dr. Leon Bruner, GMA's chief science officer, on the release today of a newNutrition Facts panel by the U.S. Food and Drug Administration (FDA):

(WASHINGTON, DC) In comments today before the U.S. Food & Drug Administration's public meeting on the import safety provisions of the FDA Food Safety Modernization Act, Dr. Leon Bruner, Chief Science Officer for the Grocery Manufacturers Association (GMA), stressed the importance of enhancing the safety and reliability of the supply chain for imported food and food ingredients.

(WASHINGTON, DC) The Grocery Manufacturers Association (GMA) today issued the following statement in response to the launch of the US Food & Drug Administration's (FDA) new consumer - friendly website for food and other product recalls:

(WASHINGTON, DC) In comments today before the U.S. Food & Drug Administration (FDA) Food Advisory Committee Meeting on certified color additives and hyperactivity in children, the Grocery Manufacturers Association (GMA) made the following statement:

I am so excited to introduce today's expert Dr. Frank Nice, a Pharmacist and Project Manager at the Food and Drug Administration and author of the book «Nonprescription Drugs for the Breastfeeding Mother».

A broad range of health professionals and scientists, including the U.S. National Academy of Sciences, the U.S. Food and Drug Administration, the American Medical Association, and the World Health Organization agree that the genetically modified foods and ingredients currently available and on the market today are safe to consume.

PFC was one of the initial study sites for FDA approval of the Follistim Pen, an FSH medication delivery device that today has made fertility drug administration much easier and comfortable for patients and is now widely used for ovarian stimulation.

The statement read in part: «As at today, the National Agency for Food and Drug Administration and Control (NAFDAC) and National Environmental Standards and Regulations Enforcement Agency (NESREA) have paid N5.5 million and N10.8 million respectively for outright purchase of the properties they are occupying.

The research, published today in Nature Neuroscience, demonstrated that brief treatment with a very low dose of romidepsin, a Food and Drug Administration - approved anti-cancer drug, restored social deficits in animal models of autism in a sustained fashDrug Administration - approved anti-cancer drug, restored social deficits in animal models of autism in a sustained fashdrug, restored social deficits in animal models of autism in a sustained fashion.

Today, alternative therapies including traditional Chinese herbal medicines (TCHM) have achieved astonishing popularity even though they are not encouraged by the U.S. Food and Drug Administration, which classifies most plant drugs as dietary supplements or food additives and also places severe limitations on labelling.

A federal court today chided the U.S. Food and Drug Administration for putting politics before science in assessing Plan B, the emergency contraceptive.

Today the U.S. Food and Drug Administration (FDA) announced that it would not ban the chemical from food and beverage containers.

The fallout continues from a decision to halt controversial cancer trials at Duke University last year: In an article today, The Cancer Letter is reporting that the U.S. Food and Drug Administration (FDA) is auditing data related to the trials.

Earlier today, the U.S. Food and Drug Administration announced that it was giving the green light to Provenge, a treatment for advanced prostate cancer that has spread to other parts of the body.

In the United States, the Food and Drug Administration (FDA) today held a public meeting to discuss draft changes it proposed in February to its Nutrition Facts label, the cliff notes summarizing the amount of fats, protein, carbohydrates, sugars, and more found in food and beverages.

Count the U.S. Food and Drug Administration (FDA) among the winners in today's budget agreement.

«Manufacturers and NIH have been working together to plan these studies,» chief scientist Jesse Goodman of the Food and Drug Administration said at the briefing today.

A joint committee of endocrinology, drug safety, and diabetes experts advising the Food and Drug Administration (FDA) split its vote today on whether to recommend removing the drug from the U.S. mardrug safety, and diabetes experts advising the Food and Drug Administration (FDA) split its vote today on whether to recommend removing the drug from the U.S. marDrug Administration (FDA) split its vote today on whether to recommend removing the drug from the U.S. mardrug from the U.S. market.

A fast - growing salmon developed by AquaBounty Technologies today became the first genetically modified (GM) animal to win the blessing of the U.S. Food and Drug Administration (FDA).

After 4 months of delay, the U.S. Senate today approved cardiologist and clinical trialist Robert Califf, President Obama's pick to head the Food and Drug Administration (FDA).

Today (Feb. 27), the Food and Drug Administration announced plans to update nutrition labels to better reflect the latest nutrition science, and the growing understanding of the link between diet and chronic diseases, the agency said.

The Food and Drug Administration approved tacrolimus in 1994, and today it is used in roughly 80 percent of kidney and 90 percent of liver and pancreas transplants.

City of Hope will be the one of the first authorized centers in the nation to provide axicabtagene ciloleucel, which the U.S. Food and Drug Administration (FDA) announced today is the first approved CAR T therapy for adult patients who have not responded to or who have relapsed after at least two other kinds of treatment.

Today, the President signed into law S. 3187, the «Food and Drug Administration Safety and Innovation Act.»

May 3, 2006 deCODE genetics (Nasdaq: DCGN) today announced that it has reached an agreement with the US Food and Drug Administration (FDA) on the design of its Phase III clinical trial for DG031, deCODE's lead developmental compound for the prevention of heart attack...

Chicago, Ill., July 20, 2016 — AveXis, Inc., a clinical - stage gene therapy company developing treatments for patients suffering from rare and life - threatening neurological genetic diseases, today announced the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation for AVXS - 101, the company's lead development candidate for the treatment of spinal muscular atrophy (SMA) Type 1 in pediatric patients.

University of Pennsylvania immunotherapy researcher Dr. Carl June, who led the development of an experimental therapy for advanced childhood leukemia that is expected to become the first CAR T - cell therapy to win U.S. Food and Drug Administration approval, will give the keynote talk today at the Conference on Cell & Gene Therapy for HIV Cure at Fred Hutchinson Cancer Research Center.

NEW YORK, NY — March 25, 2011 — The U.S. Food and Drug Administration (FDA) announced today its approval of a new treatment for advanced melanoma, the deadliest and most difficult - to - treat form of skin cancer.

The Food and Drug Administration announced a recall of Nestle Toll House refrigerated cookie dough today due to contamination with E. coli O157: H7, a type of bacteria that can cause cramps, vomiting, blood diarrhea, and a more serious condition that can result in kidney failure.