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About 1058 results for "food drug administration"

FDA decision may make Chagas treatment even more expensive
Humanosphere

FDA decision may make Chagas treatment even more expensive

The U.S. Food and Drug Administration is backing a fast-track approval process for a drug used to treat Chagas disease, but some say this approval process has a history of making drugs too expensive to help those who need it most. The ... Humanosphere, 47 minutes ago
What the FDA Approves — and What It Doesn't 24/7 Wall St, 3 hours ago
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1,150 images for food drug administration

PharmaVOICE, 1 week ago
EagleOnline.com.ng, 1 week ago
Houston Chronicle, 6 days ago
Nigeria Today.ng, 6 days ago
FOXBusiness.com, 1 week ago
FOXBusiness.com, 1 week ago
FOXNews.com, 1 week ago
Pharma Focus Asia, 3 weeks ago
Indian Express, 2 weeks ago
National Hog Farmer, 1 week ago
Time

New FDA Chief Should Have Medical Experience, Drugmakers Say

President-elect Donald Trump's pick to lead the U.S. Food and Drug Administration should have a medical background, and the agency should continue evaluating new medications effectiveness, drugmaker executives said in comments indicating opposition ...
 Bloomberg2 hours ago JUVÉDERM VOLBELLA XC...  MedEsthetics Magazine4 hours ago FDA approves generic version of Jazz Pharma's sleep disorder drug  Sharenet4 minutes ago FDA is making progress inspecting foreign drug plants, but could do better  StatNews.com1 hour ago
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LymphomaNewsToday.com

Combo Therapy for CLL, Now in Phase 3 Study, Named Orphan Drug by FDA

The U.S. Food and Drug Administration has designedthe combination of TG-1101 and TGR-1202 an Orphan Drugas a potential treatment forpeoplewith chronic lymphocytic leukemia (CLL). The therapy, developed by TG Therapeutics , is currently being ...
 LymphomaNewsToday.com8 hours ago Corbus Pharmaceuticals Receives Orphan Designation for JBT-101 for the Treatment of Systemic Sclerosis in the European Union  Financial Buzz23 minutes ago Remedy Pharmaceuticals, Inc. Release: CIRARA Granted Orphan Drug Designation For Treatment Of Severe Cerebral Edema Caused By Acute Ischemic Stroke  BioSpace6 hours ago Remedy Pharmaceuticals CIRARA Granted Orphan Drug Designation For Treatment of Severe Cerebral Edema Caused By Acute Ischemic Stroke  Business Wire7 hours ago
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Incyte PDUFA Date Pushed Back, JMP Discusses Impact

There has been a three-month delay in the Food and Drug Administration Prescription Drug User Fee Act date for Incyte Corporation (NASDAQ: INCY )'s partnered rheumatoid arthritis drug, baricitinib. The U.S. approval and launch of the drug is now ...
 Benzinga.com8 hours ago

FDA clears Vitros automation solutions, 1/17

Home » MARKETPLACE , Marketplace Archives January 2017— Ortho Clinical Diagnostics announced that the Food and Drug Administration has cleared its Vitros Automation Solutions for use with Ortho's Vitros chemistry, immunodiagnostics, and ...
 CAP TODAY18 minutes ago MindChild Medical, Inc. Announces Clearance of a 510(k) Pre-Marketing Notification with the US Food and Drug Administration (FDA) for the MERIDIAN M110 Fetal Monitoring System  Minyanville11 hours ago MINDCHILD MEDICAL, INC. : Announces Clearance of a 510(k) Pre-Marketing Notification with the US Food and Drug Administration (FDA) for the MERIDIAN M110 Fetal Monitoring System  4 Traders11 hours ago
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ZipLine® Medical Receives China Food and Drug Administration (CFDA) Approval for Non-Invasive Zip® Skin Closure System

ZipLine® Medical , Inc., an innovator in skin closure, today announced China Food and Drug Administration (CFDA) approval and commercial availability of its Zip® Surgical Skin Closure device in the region. This clearance will give the company ...
 Medical Design Technology3 hours ago Safety Warning Against Consumption Of Plasticizer-Tainted Bottle Tartare Sauce By Hong Kong Centre For Food Safety  NAFDAC6 hours ago China's food safety rate at 96.8 pct in 2016  Xinhua News Agency1 day ago Nationwide test results  Shanghai Daily1 day ago
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MedEsthetics Magazine

FDA Calls for More...

The U.S. Food and Drug Administration (FDA), which relies heavily on the results from clinical trials, is encouraging more patients to participate in trials—particularly people of all ages, races, ethnic groups and genders—as it will give the ...
 MedEsthetics Magazine21 hours ago FDA Developing Requirements For Evaluation Of Tech-Enabled Clinical Algorithms  Open Minds.com1 day ago Display caffeine content info on containers: FDA to McDonald's  Business Standard1 week ago
India-West

Indian American could be FDA head under Trump

Indian-American biotech entrepreneur Balaji Srinivasan is being considered for a role in the U.S. Food and Drug Administration (FDA) under President Donald Trump, the transition team said. Mr. Srinivasan, who is currently CEO and co-founder of ...
 The Hindu1 day ago Indian American Founder of Bitcoin Startup May Be Up for Food and Drug Administration Post  India-West23 hours ago Indian American on Trump probables list for USFDA chief  Business Line7 hours ago Indian American Balaji Srinivasan could be Trump's FDA Commissioner pick  The American Bazaar9 hours ago
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BRIEF-Spineguard gets FDA clearance for its dynamic surgical guidance integration module

n"Jan 16 Spineguard Sa * Has received 510(k) clearance from U.S. Food and Drug Administration (FDA) for its new dynamic surgical guidance integration module to be used in combination with Zavation's spinal fusion system to make its pedicle screws ...
 Reuters UK1 day ago SpineGuard secures FDA 510(k) clearance for DSG integration module to make pedicle screw smart Jan 17  Medical Device Network7 hours ago FDA approves SpineGuard's DSG integration module to make pedicle screws smart  Medical Devices Business Review14 hours ago
4 Traders

FDA extends review period by three months for rheumatoid arthritis candidate baricitinib

The US Food and Drug Administration (FDA) has extended the Prescription Drug User Fee Act (PDUFA) goal date by three months for investigational rheumatoid arthritis treatment, Baricitinib. Baricitinib is being co-developed by Eli Lilly and Company ...
 Pharmaceutical Business Review1 day ago Allergan moves toward NDA after uterine fibroid drug's success  BioPharma Dive4 hours ago FDA delays decision on Lilly and Incyte's arthritis drug  BioPharma Dive4 hours ago US FDA extends review period for Eli Lilly and Incyte's rheumatoid arthritis treatment  Pharmaceutical Technology1 day ago
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