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About 1087 results for "food and drugs administration"

FDA Approves First Drug to Treat Duchenne Muscular Dystrophy
Monthly Prescribing Reference

FDA Approves NATRELLE INSPIRA Cohesive Breast Implants

Allergan has announced that it's received approval from the U.S. Food and Drug Administration (FDA) to market NATRELLE INSPIRA Cohesive breast implants for women undergoing reconstruction, augmentation or revision surgery. The implants combine a ... MedEsthetics Magazine, 3 hours ago
FDA approves artificial pancreas system HME News, 6 hours ago
FDA Approves First Drug to Treat Duchenne Muscular Dystrophy Monthly Prescribing Reference, 2 days ago

1,910 images for food and drugs administration

International Business Times, 23 hours ago
PharmaVOICE, 1 week ago
Earth Justice, 1 week ago
Reuters India, 9 hours ago
ITechPost, 16 hours ago
WJCT, 1 day ago
Cancer Therapy Advisor, 1 week ago
Reuters India, 3 days ago
MSN News US, 1 day ago
California Healthline, 1 day ago
Washington Post

When Drug Reviewers Leave The FDA, They Often Work For Pharma

More than a quarter of the Food and Drug Administration employees who approved cancer and hematology drugs from 2001 through 2010 leftthe agency and now work or consult for pharmaceutical companies, according to research published by a prominent ...
 Washington Post2 days ago It's a Big Problem When The FDA's Drug Reviewers Keep Leaving To Work For Big Pharma  BioSpace1 day ago Many ex-FDA drug reviewers take revolving door to pharma industry  MedCity News1 day ago FDA drug reviewers often end up at pharma companies  HealthImaging12 hours ago

Misbranded drugs worth Rs 18 lakhs seized

The officers of the vigilance branch of the Food and Drugs Administration (FDA) led by FDA Joint Commissioner Harish Baijal, raided the godown of 'Shree Rajchem', located at Kisturi Complex in Bhiwandi, Thane district, on Tuesday. Mis-branded drugs ...
 Afternoon Despatch & Courier1 week ago Adulterated mawa worth Rs 9 lakh seized  Asian Age3 weeks ago Gutkha unit unearthed; machines, goods worth Rs 1.5cr seized  Business Standard2 months ago

Maha FDA detects Mumbai based firm selling spurious drugs

In its ongoing drive against illegal sale of medicines, the Maharashtra Food and Drug Administration (FDA) has seized stock of active pharmaceuticals ingredients (API) from a Mumbai-based firm which was selling drugs without proper purchase invoices ...
 PharmaBiz6 days ago Maha FDA seizes fakes of popular soaps from Mumbai mfg unit  Money Control1 month ago FDA raids Mumbai factory manufacturing duplicate soap  Business Standard1 month ago

Brooks Lab up 17% on manufacturing licence for Gujarat plant

The Commissioner of Food Drugs Control Administration, Gandhinagar has granted manufacturing licence to the company's new manufacturing facility at Vadodra, Gujarat to manufacture of pharmaceutical products.
 Money Control3 weeks ago Wockhardt slumps as USFDA issues import alert on the company's Ankleshwar unit  Business Standard1 month ago Wockhardt falls 14 pct on import alert; Macquarie downgrades  Business Standard1 month ago Wockhardt slumps 10%  India Infoline1 month ago
Money Control

USFDA warns Pan Drugs for violations of CGMP norms

In a warning letter to Pan Drugs MD and Chairman Kamal Pandya, US Food and Drug Administration (USFDA) said the company's "methods, facilities, or controls for manufacturing, processing, packing, or holding do not conform to CGMP, your drug products are ...
 Money Control3 weeks ago

U.S. FDA approves Amgen's copy of AbbVie arthritis drug Humira

(Adds details, background) WASHINGTON, Sept 23 (Reuters) - The U.S. Food and Drug Administration on Friday approved Amgen Inc's biosimilar version of AbbVie's top-selling arthritis drug, Humira. Amgen's drug, Amjevita, known also as ...
 Sharenet6 days ago FDA approves Amgen's copy of AbbVie arthritis drug Humira  FOXNews.com3 days ago UPDATE 1-U.S. FDA approves Amgen's copy of AbbVie arthritis drug Humira  Business Insider5 days ago UPDATE 2-U.S. FDA approves Amgen's copy of AbbVie arthritis drug Humira  Reuters UK6 days ago

Comparing Generic and Innovator Drugs: A Review of 12 Years of Bioequivalence Data from the United States Food and Drug Administration

Download the PDF here Abstract BACKGROUND In the US, manufacturers seeking approval to market a generic drug product must submit data demonstrating that the generic formulation provides the same rate and extent of absorption as (ie, is ...
 National AIDS Treatment Advocacy Project1 day ago More than 30 states sue drug manufacturers for blocking Suboxone generic  Healio1 day ago

3Q: Berhardt Trout on spurring innovation in drug manufacturing

When it comes to manufacturing drugs, they do make them like they used to. An April report from the Food and Drug Administration stated that today's plants differ very little from those in the 1960s. Bernhardt Trout would like to change that. The ...
 PressReleasePoint3 days ago Novartis AG-MIT Exec On Spurring Innovation In Drug Manufacturing  BioSpace3 days ago
Federal Register

FDA Issues Draft Guidance on Coordinated Development of Antimicrobial Drugs and Antimicrobial Susceptibility Test Devices- Drug Information Update

The U.S. Food and Drug Administration has released a draft guidance document entitled Coordinated Development of Antimicrobial Drugs and Antimicrobial Susceptibility Test Devices. This draft guidance is intended to help drug sponsors and device ...
 American Pharmaceutical Review1 week ago Coordinated Development of Antimicrobial Drugs and Antimicrobial Susceptibility Test Devices; Draft Guidance for Industry and Food and Drug Administration Staff; Availability  Federal Register1 week ago FDA issues draft guidance for the coordinated development of antimicrobial drugs and antimicrobial susceptibility test devices  Healthcare Purchasing News6 days ago
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