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About 1071 results for "food drug administration"

US FDA issues complete response letter to Bristol-Myers for da...

Bristol-Myers Squibb Company announced that the US Food and Drug Administration (US FDA) has issued a Complete Response Letter (CRL) regarding the New Drug Application (NDA) for daclatasvir, an NS5A complex inhibitor, in combination with other ... PharmaBiz, 20 hours ago
Avanir receives FDA CRL for drug-device combination product AVP-825 Medical Devices Business Review, 11 hours ago
Avanir's AVP-825 NDA gets FDA complete response letter Pharmaceutical Business Review, 9 hours ago

278 images for food drug administration, 3 days ago, 1 week ago
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Farm Futures, 2 days ago, 1 week ago
Monthly Prescribing Reference

Weight Loss Caps Contain Withdrawn Drug

Share this article: The Food and Drug Administration (FDA) is warning consumers to not buy or use Slim-Vie, a supplement marketed for weight loss . Slim-Vie capsules were found to contain sibutramine , a controlled substance that was withdrawn ...
 Monthly Prescribing Reference2 days ago FDA Notifies Consumers Not to Use Bee Slim: AttorneyOne Monitors and Keeps Consumers Informed  Red Orbit13 hours ago FDA Ruling Provides Consumers with Calorie Labeling Information to Make Informed Food Choices  Reliance Trust3 days ago Drug Information Update- Feng Shi Ling contains undeclared drug ingredients  Food Consumer6 days ago

New test to be used for Ebola prevention in China

China Food and Drug Administration (CFDA) has approved three home-grown Ebola test reagents to be used in prevention of the speread of the virus. The three test reagent products are made by Daan Gene Co., Ltd of Sun Yat-Sen University, Shenzhen ...
 Individual.com8 hours ago China approves new Ebola prevention drugs  Nigeria Punch4 hours ago China to use new test to prevent Ebola  Business Standard India7 hours ago

Ipsen Says FDA Accepts For Review SBLA For Dysport

Ipsen SA (IPSEY: Quote) said the U.S. Food and Drug Administration has accepted for review its supplemental Biologics License Application or sBLA for Dysport (abobotulinumtoxinA) in the treatment of upper limb spasticity in adult patients. The ...
 RTTNews.com18 hours ago Ipsen's Dysport accepted for review by US FDA  Pharma Letter7 hours ago Ipsen Announces FDA Acceptance of Filing for Dysport® in the Treatment of Upper Limb Spasticity in Adult Patients  Investor's Business Daily17 hours ago

FDA to weigh lifting ban on gay men donating blood

Advisors for the Food and Drug Administration (FDA) will meet next week to discuss lifting a 30-year-old ban that prohibits gay men from donating blood. Long-time critics of the ban, including some members of Congress, say the Dec. 2 meeting is a ...
 FOXNews.com8 hours ago

Gujarat FDCA plans to set up medical device testing lab in the state

The Gujarat Food and Drug Control Administration(FDCA) is contemplating to set up a medical device testing laboratory in the state, soon, if things go as planned. The state drug regulator is currently in discussion with the Centre and the state ...
 PharmaBiz16 hours ago

US FDA allows marketing of HeartFlow FFR-CT device to help heart blood flow

The US Food and Drug Administration has allowed marketing of the HeartFlow FFR-CT software, which permits health care professionals to non-invasively evaluate blood flow in the coronary arteries of patients showing signs and symptoms of coronary ...
 PharmaBiz17 hours ago
Reuters India

United States : Novartis announces extension to FDA review period for multiple myeloma investigational compound LBH589 [TendersInfo (India)]

Novartis announced today that the US Food and Drug Administration (FDA) has extended their priority review period by up to three months for the new drug application (NDA) of LBH589 (panobinostat) in combination with bortezomib* and dexamethasone for ...
 Pharmacy Choice16 hours ago Novartis says U.S. FDA extends review period for bone marrow drug  Reuters3 days ago FDA Delays Approval For Novartis AG (NVS) Myeloma Drug  Bidness Etc3 days ago US Food and Drug Administration extends review period for bone marrow drug- Novartis  Economic Times3 days ago

Sweeping changes: FDA strengthens calorie-posting requirements

On Tuesday, Nov. 25, the Food and Drug Administration (FDA) released new requirements about calorie labeling that would stretch even into movie theaters and bars. Menu labeling was part of the 2010 Affordable Care Act (ACA), requiring chain ...
 Examiner.com22 hours ago FDA summarizes labelling requirements for restaurants, vending machines  Canadian Vending1 day ago Fast food mystery no more: FDA releases sweeping new calorie labeling rules  Salon3 days ago

FDA Advisory Panel Votes on Epidural Steroid Shots for Pain

WEDNESDAY, Nov. 26, 2014 (HealthDay News) -- An expert advisory panel to the US Food and Drug Administration decided on Tuesday not to recommend the agency issue a strong warning against the general use of steroid injections for neck or back pain; ...
 HCPLive2 hours ago FDA panel backs Daiichi's blood thinner  Reuters4 weeks ago FDA staff recommends limited use of Daiichi's blood thinner  Reuters1 month ago FDA panel votes to expand use of Vertex cystic fibrosis drug  Reuters1 month ago
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