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Today Sue Sutter Please Login to read the full article. Full Article at Scrip News
Today Asher Mullard Please Login to read the full article. Full Article at Scrip News
From left, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention Director Dr. Anne Schuchat, Assistant Health and Human Services Secretary for Preparedness and Response, Dr. Nicole Lurie; and Acting Chief... View Photo »
This is a safety issue and we are asking the FDA to act quickly to protect consumers ... Most of the ads for alcoholic energy drinks are aimed at young people and all of the research indicates these drinks put young people at great risk.
More than five years ago, one of California's leading hospitals decided to leap into the future of medical care by digitizing its patients' health records. Full Article at Huffington Post
Orexigen cautions you that statements included in this press release that are not a description of historical facts are forward-looking statements. Words such as "believes," "anticipates," "plans," "expects," "indicates," "will," "intends," "potential," Full Article at RedOrbit
BioSpecifics Technologies Corp. is a biopharmaceutical company that has developed injectable collagenase for eleven clinical indications, three of which include: Dupuytren's disease, Peyronie's disease, and frozen shoulder (adhesive capsulitis). Full Article at RedOrbit
"Covidien (NYSE: COV), a leading global provider of healthcare products, today announced the launch of DuraSeal(TM) spine sealant, the first product approved by the FDA for intra-operative sealing of the dural membrane during spine procedures." View Photo »
The FDA approval of Geodon provides an additional treatment option for patients with bipolar disorder, who require maintenance therapy to keep the symptoms of the disease under control
MINNEAPOLIS, Nov. 24 /PRNewswire/ -- Ecigazon.com, an Electronic Cigarette company and advocate for Electronic Cigarettes as an alternative to tobacco smoking, has sent its own Health Reform to the White House: an Electronic Cigarette as a gift to... Full Article at RedOrbit
On 11/23/09, Transcept Pharma (TSPT) announced that it is scheduled to meet with the FDA on 1/20/10 to discuss the Complete Response Letter (CRL) regarding the New Drug Application (NDA) for Intermezzo (zolpidem tartrate sublingual tablet). Full Article at ETF Investor
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 cosmeti... Full Article
From left, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention Director Dr. Anne Schuchat, Assistant Health and Human Services Secretary for Preparedness and Response, Dr. Nicole Lurie; and Acting Chief Scientist FDA Dr. Jesse Goodman, a...
View Photo »"Covidien (NYSE: COV), a leading global provider of healthcare products, today announced the launch of DuraSeal(TM) spine sealant, the first product approved by the FDA for intra-operative sealing of the dural membrane during spine procedures."
View Photo »Tilapia fish gather at a viewing window in their holding tank at the U.S. Food and Drug Administration's (FDA) Center for Veterinary Medicine labs in Laurel, Maryland, November 5, 2009.
View Photo »Staff walk among the new buildings at the the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »Plants are lined up to be planted among new buildings at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »A high resolution digital scan shows the cell-level detail of a rat's kidney during a tour of the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »A high-magnification microscope is shown during a tour of the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »A digital scan of a rat kidney is shown on a screen at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »A rat genome gene chip is shown to the media by Karol Thompson, Lead Pharmacologist in the Molecular Toxicology lab at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009. Watching on is biologist Barry Rosenzweig.
View Photo »An illustration of a kidney and samples are shown in the Investigational Pathology lab at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »Rodney Rouse, Veterinary Medical Officer at the U.S. Food and Drug Administration (FDA), shows a chart of biology scans to science industry writers at the FDA headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »Jun Zhang, Toxicologic Pathologist/Pharmacologist at the U.S. Food and Drug Administration (FDA), speaks to the media alongside a digital scan of a kidney during a tour of the FDA headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »A slide of rat kidneys are prepared for digital scanning for medical analysis at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »A rat genome gene chip is shown in the Molecular Toxicology lab at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »Rat genome gene chips are shown in the Molecular Toxicology lab at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 5, 2009.
View Photo »A science writer wears a pair of polarized glasses to view a Polarization Stereoscopic display during a tour of the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 4, 2009.
View Photo »Dr Aldo Badano shows images of real human breast (R) and an computer-generated one (2nd R) during a demonstration of computational models of 3D novel 3D breast imaging systems at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 4, 2009.
View Photo »Dr Aldo Badano shows images of a fake (L) and real human skeleton during a demonstration of computational models of 3D imaging systems at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 4, 2009.
View Photo »Science writers are giving a tour of an electromagnic environment chamber during a tour of the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 4, 2009.
View Photo »A new building is shown during construction at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 4, 2009.
View Photo »The headquarters of the U.S. Food and Drug Administration (FDA) is shown in Silver Spring, Maryland, November 4, 2009.
View Photo »An image of a human skull is shown in a Polarization Stereoscopic display during a tour of the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 4, 2009.
View Photo »A laboratory staff conducts an experiment in a Magnetic Resonance Imaging (MRI) chamber inside a lab at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 4, 2009.
View Photo »The headquarters of the U.S. Food and Drug Administration (FDA) is seen in Silver Spring, Maryland November 4, 2009.
View Photo »Biosensors, involving fluorescence resonance energy transfer using peptide substrates, glow in different colours during a lab tour for media from the science industry at the U.S. Food and Drug Administration (FDA) headquarters in Silver Spring, Maryland, November 4, 2009.
View Photo »"Covidien (NYSE: COV), a leading global provider of healthcare products, today announced the launch of DuraSeal(TM) spine sealant, the first product approved by the FDA for intra-operative sealing of the dural membrane during spine procedures."
View Photo »This is a safety issue and we are asking the FDA to act quickly to protect consumers ... Most of the ads for alcoholic energy drinks are aimed at young people and all of the research indicates these drinks put young people at great risk.
The FDA approval of Geodon provides an additional treatment option for patients with bipolar disorder, who require maintenance therapy to keep the symptoms of the disease under control
Manufacturers urgently need a way to discuss end-to-end product development plans with the FDA (U.S. Food and Drug Administration) or its advisory boards early in the product development process
The FDA works in close collaboration with our regulatory and law enforcement counterparts in the United States and throughout the world to protect the public
We applaud the HELP Committee for its bipartisan approval of the bill which will provide the U.S. Food and Drug Administration (FDA) with the resources and authorities the agency needs to help make prevention the focus of our food safety strategies.
Many of our clients believed the FDA had evaluated Zicam before it reached the market ... In fact, Zicam products were not regulated or approved by the FDA because they were listed as homeopathic treatments that use natural ingredients. Mounting evidence from the scientific community is proving Zicam wi...
Many of our clients believed the FDA had evaluated Zicam before it reached the market ... In fact, Zicam products were not regulated or approved by the FDA because they were listed as homeopathic treatments that use natural ingredients. Mounting evidence from the scientific community is proving Zicam wi...
Medtronic remains committed to providing the highest quality products to our customers and is working with FDA to resolve all remaining issues as quickly as possible
The FDA views the two medicines as so interchangeable that the agency recently approved Lexapro's use in depressed adolescents based in part on the results of a study Forest conducted using Celexa.
We look forward to working with the FDA to evaluate the data from more than 2,600 women with advanced breast cancer who participated in these studies that showed Avastin in combination with various chemotherapies helped them live longer without the disease worsening
We have made significant progress in bringing the Allston plant back in operation, and we will continue to work closely with the FDA to resolve these issues
Banning fresh Gulf oysters in the name of food safety is like killing a fly with a sledgehammer ... Now it appears the FDA is coming to realize the harm this ban could have on Louisiana and is reaching for a fly swatter instead. I am pleased the FDA has listened to the arguments we in Louisiana have bee...
Banning fresh Gulf oysters in the name of food safety is like killing a fly with a sledgehammer ... Now it appears the FDA is coming to realize the harm this ban could have on Louisiana and is reaching for a fly swatter instead. I am pleased the FDA has listened to the arguments we in Louisiana have bee...
While it's a victory, the FDA stepping back from implementing the new policy, we still have to be careful because they've yet to altogether rule out a ban on raw oysters from the Gulf Coast
These products have not been approved, cleared or otherwise authorized by FDA for use in the diagnosis, mitigation, prevention, treatment or cure of the H1N1 flu virus
The FDA's decision today is a major win for our oyster industry and all of Louisiana
While some of the entry's content may repeat the sponsor's own labeling or advertising, Wikipedia users can alter this content and post additional information ... As a result, the final Wikipedia page may - through no fault of the sponsor - fail to comply with FDA advertising and labeling rules were the...
We remain confident in our NDA submission and will continue to work closely with the FDA toward the potential approval of intravenous acetaminophen
We are making the necessary preparations to initiate a Phase III trial to submit a new drug application (NDA) to the U.S. Food and Drug Administration (FDA) to commercialize DAVANAT®
This research further underscores the value of online and social media and confirms it is not just a fad for a select group of consumers ... Social media has instead become more relevant in consumer communications, not only supporting offline social dialogues but also allowing people to research and see...
The FDA's licensure of CSL Biotherapies' thimerosal-free monovalent pandemic H1N1 vaccine for use in children aged 6 months and older is a critically important milestone ... The U.S. Centers for Disease Control has identified young children as a priority group for pandemic H1N1 vaccine administration. C...
By approving information to be included in the drug labeling, the FDA has determined that the information complies with its rules and regulations. Therefore, if the FDA labeling supports the statements made in the advertising for an FDA-approved drug, the statements are not actionable under the (Arkansa...
PocketCPR® for iPhone is a training app and is not cleared by the FDA for rescue use. With over 40 million iPhones and iPod Touches in use, providing an easy-to-use application through which the public can learn CPR could significantly help improve outcomes from SCA, the leading cause of unexpected deat...
Fake organic personal care products cut across three jurisdictions – the federal trade commission (FTC) as this is a mislabelling issue, the USDA and the FDA. Any of these three or a combination thereof should take action
The Center represents probably the first opportunity in the history of cardiac safety where data of this scale and value has been gathered together and made available to academic and industry researchers ... At the same time, these resources will help support a scientific network in which ideas and conc...
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