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About 1068 results for "food and drugs administration"

NAFDAC Strikes Masterminded By Fake Drug Importers DG

— Nov 20, 2014 | The director-general of the National Agency for Food, Drug Administration and Control (NAFDAC) Dr Paul Orhii has disclosed that the ongoing strike action embarked upon by his workers could be mastermind by fake drug importers. ... Leadership, 6 days ago
Customs, NAFDAC Destroy N348 Million Drugs, 2 hours ago
NAFDAC arrests 10 over forgery, fake drugs Nigeria Daily Independent, 6 days ago

266 images for food and drugs administration, 1 day ago, 4 days ago
NPR, 6 days ago
The Nation Nigeria, 2 days ago
Malaysian Insider, 12 hours ago
Bayou Buzz, 1 hour ago
WBUR, 3 hours ago
Farm Futures, 4 hours ago, 1 week ago
Deutsche Welle, 6 days ago

Pharmaceutical Newsletter - November 17 to 21, 2014

Ranbaxy Laboratories Ltd has sued US Food and Drug Administration (FDA) for revoking approvals granted to the firm to launch copies of two drugs including AstraZeneca Plc's heartburn pill Nexium, according to reports. Top News Aurobindo Pharma's director ...
 India Infoline5 days ago RANBAXY LABORATORIES : Sues usfda for revoking drug approvals  4 Traders6 days ago Ranbaxy sues FDA on permits  Asian Age1 week ago Ranbaxy Lab drops after reports of suing USFDA for revoking drug approvals  Business Standard1 week ago
Bidness Etc

European Commission - European Medicines Agency - China Food and Drugs Administration bilateral and International Summit of Heads of Medicines Regulatory Agencies, Beijing, China, From: 17-Nov-2014, To: 21-Nov-2014

Summary The European Union China Working Group on Pharmaceuticals, which brings together the European Medicines Agency (EMA), the European Commission (EC) and the China Food and Drugs Administration, meets on 18 November to progress discussions on ...
 European Medicines Agency6 days ago Sanofi SAs (SNY) Oral Gaucher Disease Drug Backed By European CHMP  Bidness Etc4 days ago

Sterilisation deaths: Drug company had faced action earlier

In 2010-11, the Food and Drug Administration had cancelled 'product permission' of six drugs manufactured by the company for being substandard, a senior official of FDA told PTI. Subsequently, in 2012, two cases were filed against the company in the court of ...
 Economic Times1 week ago

Paneer, milk cream worth Rs 11.67 lakh seized

Officials of the Food and Drug Administration (FDA) on Sunday seized a stock of paneer (cottage cheese) and cream worth Rs 11.67 lakh brought to Pune from Karnataka in an unhygienic condition.The stock was destroyed.
 Times of India2 weeks ago Gutkha worth Rs 4.5L seized from Ghodbunder road  Times of India3 weeks ago Unit using old tins for edible oil closed down  Times of India2 months ago FDA seizes gutka, paan masala  Times of India2 months ago

US regulator fast-tracks approval for Wockhardt drugs

Mumbai-based Wockhardt Ltd has received Qualified Infectious Disease Product (QIDP) status from the US Food and Drug Administration (FDA) for two of its drugs, WCK 771 and WCK 2349. WCK 771 is an intravenous (IV) drug while WCK 2349 is a solid oral tablet, under anti-infective category. The drugs were also granted five-year extension to the drug patents in the US. A QIDP status is granted to drugs which act against pathogens which have a high degree of unmet need in their treatment and are ...
 Rediff.com2 months ago USFDA grants QIDP status to two Wockhardt drugs  Money Control2 months ago Wockhardt gains as USFDA grants QIDP status to two drugs  Business Standard2 months ago Wockhardt surges 6%, only Indian co to receive QIDP status  Money Control2 months ago

FDA initiates survey to gauge shortage of chicken pox vaccine

The Food and Drugs Administration (FDA) officials on Tuesday initiated a three-day long market survey to find out the exact shortage of chicken pox vaccine in the city.
 Times of India2 months ago

US FDA issues additional guidance for outsourcing facilities that compound sterile human drugs

The US Food and Drug Administration issued three additional policy documents to assist entities that compound sterile human drugs with registering as outsourcing facilities. The policy documents will also assist entities with complying with ...
 PharmaBiz1 day ago FDA issues additional guidance for outsourcing facilities that compound sterile human drugs  U.S. Food and Drug Administration4 days ago

Funding Opportunity for Minor Use/Minor Species (MUMS) Development of Drugs to Publish in Early 2015

The Food and Drug Administration (FDA) will publish a New Funding Opportunity Announcement (FOA) entitled Minor Use Minor Species Development of Drugs; Research Project Grant (R01) in early 2015. The new FOA will replace #RFA-FD-12-003, which is set ...
 ALN23 hours ago

Sun Pharma recalls 68194 bottles of anti-depression drug in US

Report stated that company withdrew the drugs, after failed to dissolve properly, US Food and Drug Administration says. Sun Pharmaceuticals has recalled about 68,000 bottles of its anti-depressant venlafaxine hydrochloride, from the US market, says report.
 India Infoline1 week ago
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