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About 1178 results for "food drug administration"

UPDATE 1-Salix's constipation drug gets approval for expanded use

(Adds detail, analyst comment, shares) By Natalie Grover (Reuters) - Salix Pharmaceuticals Ltd said the U.S. Food and Drug Administration approved an expanded use of its constipation treatment. The injection, Relistor, has now been approved ... Reuters, 2 days ago
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1,282 images for food drug administration

News 9, 8 hours ago
Daily Caller, 1 hour ago
ADVFN UK, 6 hours ago
Yahoo! Finance, 16 hours ago
Irish Times, 1 week ago
Colorado Springs Gazette, 2 weeks ago
KansasCity.com, 2 weeks ago
Orlando Sentinel, 3 weeks ago
KansasCity.com, 2 weeks ago
KansasCity.com, 2 weeks ago

Cytrx Corp receives multiple FDA orphan drug designations for aldoxorubicin for treatment of glioblastoma, small cell lung cancer and ovarian cancer

6:00am EDT Cytrx Corp:Says that the U.S. Food and Drug Administration (FDA) has granted multiple Orphan Drug Designations for the company's lead drug candidate, aldoxorubicin, in three indications: glioblastoma multiforme (GBM), small cell lung ...
 Reuters2 days ago CytRx Gets Multiple Orphan Drug Designations For Aldoxorubicin  RTTNews.com2 days ago US FDA grants multiple orphan drug status to CytRx's aldoxorubicin for treatment of glioblastoma, SCLC & ovarian cancer  PharmaBiz1 day ago FDA grants multiple Orphan Drug Designations for CytRxs aldoxorubicin  Big News Network2 days ago

BSD Medical's China Distributor Receives China Food and Drug Administration Marketing and Import License Approval for the BSD-2000 Hyperthermia System

Creates Sales Pathway for BSD-2000 in Largest and Most Receptive Hyperthermia End-Market in the World SALT LAKE CITY--( BUSINESS WIRE )--BSD Medical Corporation (NASDAQ:BSDM) (the Company or BSD), a leading provider of medical ...
 Business Wire2 days ago Pierre Fabre receives MA for lung and breast cancer drug in China  Individual.com2 days ago BSD MEDICAL : China Distributor Receives China Food and Drug Administration Marketing and Import License Approval for the BSD-2000 Hyperthermia System  4 Traders2 days ago
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Bristol immunotherapy gets six month U.S. FDA review for melanoma

(Reuters) - The U.S. Food and Drug Administration has granted a six-month, priority review to Bristol-Myers Squibb Co's application for immuno-oncology drug Opdivo as a treatment for previously treated melanoma, the company said on Friday. The FDA decision is ...
 Reuters5 days ago Bristol immune drug shows strong effect in melanoma study  Reuters2 days ago Another Success For Bristol-Myers PD-1 Immunotherapy Drug  Bidness Etc2 days ago UPDATE 1-Bristol immune drug shows strong effect in melanoma study  Reuters2 days ago
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FDA Grants Orphan Drug Status To Insys' Brain Tumor Treatment

Insys Therapeutics, Inc. (INSY: Quote) Monday said the U.S. Food and Drug Administration has granted orphan drug status to the company's pharmaceutical cannabidiol for treating glioma, a common type of malignant brain tumor. CEO Michael Babich said ...
 RTTNews.com2 days ago INSYS THERAPEUTICS : Receives FDA Orphan Drug Designation for Its Pharmaceutical Cannabidiol as a Potential Treatment for Glioma  4 Traders2 days ago Insys Therapeutics Inc receives FDA orphan drug designation for pharmaceutical cannabidiol as potential treatment for glioma  Reuters UK2 days ago Insys Therapeutics Receives FDA Orphan Drug Designation for Its Pharmaceutical Cannabidiol as a Potential Treatment for Glioma  Pharmacy Choice2 days ago
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Jagran Post

Scorpion-derived 'tumour paint' to fight brain cancer

venom may help fight deadly brain cancer, say US scientists who will conduct human trials of the product. The Food and Drug Administration has approved the product, developed by Blaze Bioscience, for study in human trials in the US. During the phase one ...
 Business Standard2 days ago Scorpion venom to fight brain cancer  Prokerala2 days ago

Life-saving drugs and deadly delays

The Food and Drug Administration just granted permission for expanded access to an experimental medicine for Ebola. It's OK as far as it goes, but it's an exception to the FDA's reluctance to approve the use of life-saving products. Safety and ...
 New York Post3 days ago

Oral OTEZLA® (apremilast) Approved by the U.S. Food and Drug Administration for the Treatment of Patients with Moderate to Severe Plaque Psoriasis

/Business Wire SUMMIT, N.J. Saturday, September 27th 2014 In phase III studies, OTEZLA resulted in significant and clinically meaningful improvements in plaque psoriasis OTEZLA demonstrated a consistent safety and tolerability profile ...
 Emirates Week2 days ago ORAL OTEZLA® (apremilast) é Aprovado pelo U.S. Food and Drug Administration para o Tratamento de Pacientes com Psoríase em Placas de Moderada a Grave  Business Wire6 days ago Oral OTEZLA (apremilast) Approved by the U.S. Food and Drug Administration for the Treatment of Patients with Moderate to Severe Plaque Psoriasis  Asian Hospital & Healthcare Management1 week ago Oral OTEZLAR Approved by the U.S. Food and Drug Administration for the Treatment of Patients with Moderate to Sever  Big News Network1 week ago
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Abbvie gets FDA approval for Crohn's disease drug Humira

AbbVie has received approval from the US Food and Drug Administration (FDA) for Humira (adalimumab) to reduce signs and symptoms as well as achieve and maintain clinical remission, in pediatric Crohn's disease patients six years of age and older. ...
 Pharmaceutical Business Review5 days ago AbbVie gets new approval for its drug Humira  Investor's Business Daily6 days ago Abbvie gets FDA approval for Crohns disease drug Humira  Big News Network4 days ago

FDA, DBP ink deal for faster, easier registration of new food items, drugs

The Food and Drug Administration (FDA) on Friday inked a deal with the Development Bank of the Philippines (DBP) and BancNet, Inc. that will allow business owners to pay FDA registration fees for new food and drug products through any BancNet member ...
 Business World5 days ago
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