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About 153 results for "food and drugs administration"

Food and Drugs Administration aims to speed up work using tablets
DNA

Food and Drugs Administration aims to speed up work using tablets

In order to go digital, since few years, the FDA department officials have been working on online software to give online registration and licenses to the food and drugs related applicants. DNA, 2 weeks ago

10 images for food and drugs administration

DNA, 1 week ago
DNA, 3 weeks ago
DNA, 2 weeks ago
Business Standard, 1 month ago
Money Today, 3 months ago
DNA, 3 months ago
Money Today, 5 months ago
Money Control, 5 months ago
First Post.com, 6 months ago
The Telegraph UK, 6 months ago

FDA working on a 'dozen' policies to boost copycat biotech drugs

NEW YORK (Reuters) - The U.S. Food & Drug Administration is working on around a dozen actions to boost use of cheaper versions of expensive biotech medicines, the head of the agency Scott Gottlieb said on Wednesday.
 Reuters3 weeks ago

FDA declines to approve Pfizer's biosimilar to Roche's cancer drug

(Reuters) - Pfizer Inc said on Monday the U.S. Food and Drug Administration (FDA) declined to approve the company's biosimilar to Roche's breast cancer drug, Herceptin, and sought additional technical information.
 Reuters43 minutes ago GW Pharma gets FDA panel nod, first cannabis-based drug nearing approval  Reuters3 days ago FDA needs more time to review AbbVie, Neurocrine's uterine pain drug  Reuters1 week ago FDA expands use of Amgen leukemia drug Blincyto to patients with relapse risk  Reuters3 weeks ago
Business Standard

World's first contact lenses that darken in bright light approved in US

The US Food and Drug Administration (FDA) has approved the world's first contact lens that automatically darkens when exposed to bright light.The Acuvue Oasys Contact Lenses with Transitions Light Intelligent Technology are soft contact lenses indicated for ...
 Business Standard1 week ago First Artificial Intelligence (AI) Device Approved by US FDA for Diabetic Retinopathy  Med India1 week ago US approves first AI-based device to detect diabetic eye disease  Business Standard1 week ago FDA approves marketing of first AI device to detect diabetic eye disease  Business Standard1 week ago
Business Standard

Lupin will be watched after USFDA tentative nod for testosterone gel

Drug major Lupin announced that it has received tentative approval from the United States Food and Drug Administration (USFDA) to market a generic version of AbbVie Inc's AndraGel, 1.62%. Lupin's Testosterone Gel is the generic equivalent of AbbVie Inc.'s ...
 Business Standard5 days ago Glenmark Pharmaceuticals receives ANDA approval for Clobetasol Propionate Spray  Money Control3 weeks ago Lupin stock in 2017 global worst-performer list, says Evaluate report  Business Standard1 month ago Aster DM Healthcare in focus on debut  Business Standard1 month ago
Money Control

Alkem Laboratories falls 11% as USFDA issues 13 observations to Daman plant

The Mumbai-based pharma company has received a Form 483 with thirteen observations from US Food and Drug Administration (USFDA) for Daman facility.
 Money Control3 weeks ago Alkem Labs gets 14 USFDA observations for two units  Business Standard3 weeks ago India's Alkem Labs gets USFDA report about Amaliya unit  Reuters3 weeks ago Aurobindo Pharma falls 2% after USFDA finds female mosquito in unit 4  Money Control1 month ago

Health, medical groups sue FDA over e-cigarette rule delay

(Reuters) - Seven public health and medical groups on Tuesday filed a lawsuit challenging a U.S. Food and Drug Administration decision that they said would allow e-cigarettes to remain on the market for years without regulatory review.
 Reuters3 weeks ago Vidaza generic doing well for us; market share is increasing: Shilpa Medicare  Money Control1 month ago FDA approves Sorrento's non-opioid painkiller patch, shares jump  Reuters1 month ago KemPharm's opioid painkiller gets FDA approval, shares soar  Reuters1 month ago

Strides Shasun gets USFDA nod for HIV treatment drug

The approval granted to the company#39;s wholly-owned subsidiary Strides Pharma Global Pte by the US Food and Drug Administration (USFDA) is for Efavirenz tablets of 600 mg strength, the company said in a regulatory filing.
 Money Control1 month ago US regulator's nod for Strides arm's drug to treat HIV  Prokerala2 months ago Strides Shasun arm gets USFDA nod for allergy relief drug  Business Standard1 week ago Strides Shasun gets US regulator nod for Ibuprofen capsules  Business Standard3 weeks ago
Business Standard

Dr Reddy's is awaiting 102 approvals from US Food and Drug Administration

US drug regulator raised the issue of significant deviations from the current good manufacturing practice (cGMP) in three of DRRD's plants in a letter issued in November 2015 Abhineet Kumar | Mumbai Last Updated at March 6, 2018 07:10 IST Investors in Dr ...
 Business Standard1 month ago Why Dr Reddy's expects FY19 to be stronger and richer  Rediff.com1 month ago

FDA staff cites safety issues for Lilly, Incyte's rheumatoid arthritis drug

(Reuters) - The U.S. Food and Drug Administration staff on Thursday flagged concerns about potentially fatal blood clots from higher doses of Eli Lilly and Co and Incyte Corp's rheumatoid arthritis drug.
 Reuters4 days ago FDA staff raises safety concerns over Lilly/Incyte arthritis drug  Reuters3 days ago
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