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United States Food Drug Administration

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Zika epidemic: Donated blood across US to be screened for virus

In a move to prevent transmission of the Zika virus through blood supply, the United States Food and Drug Administration has recommended that all blood donated in the country and its territories be......

Mice, roaches found in food served on US airlines: FDA

In a shocker, the United States Food and Drug Administration has discovered the presence of mice, ants and cockroaches in food served on airlines in the country. Through a Freedom of Information......

Silicone breast implants may rupture: US FDA

A United States government's Food and Drug Administration panel has warned women seeking larger breasts that up to 93 per cent of silicone implants rupture in ten years.The alternative, saline......

Maharashtra to cancel licences of gutkha cos

Acting on a report about the presence of magnesium carbonate in gutkha, the Maharashtra Food and Drug Administration on Saturday issued directives to various departments to cancel the licences of......

More worm-infested Cadbury chocolates found

Ten Cadbury chocolate bars were on Monday sent to the Maharashtra Food and Drug Administration laboratory in Dadar, Mumbai, for testing whether they contained worms.The move came three days after......

FDA warns India's Emcure Pharma, cites repeated data fudging at plant

It is one of 42 drug-making factories in India that the FDA has banned in recent years The US Food and Drug Administration (FDA) has warned Indian generic drugmaker Emcure Pharmaceuticals, saying......

US warns Novartis on manufacturing violations at 2 India plants

The US Food and Drug Administration warned Novartis AG last week after the Swiss firm was found in violation of manufacturing practices last year at two of its India drug-making plants, Novartis......

US food regulator testing Maggi noodles after India recall

The US Food and Drug Administration (FDA) is testing samples of Maggi, a Nestle instant noodle brand, which was recalled from stores across India last week, a spokeswoman for the Swiss food group......

Approval delays to hurt Indian pharma cos' US sales

Indian drugmakers expect a slowdown in new generic drug approvals by the US Food and Drug Administration (FDA) to weigh on sales in their largest market for at least two more quarters, due to an......

Regulator finds procedural lapses at Wockhardt's US facility

The US Food and Drug Administration has found as many as 12 procedural lapses in drug maker Wockhardt's US facility in Illinois.           The inspection, which was......

Sharapova's intent questioned - Why was she taking banned heart drug?

'Sharapova has been a US resident since early in her career, which does bring in a question of how or why she is using a drug that is not licensed there' IMAGE: Maria Sharapova speaks to the media......

What is meldonium? Why did Sharapova use it?

IMAGE: Maria Sharapova prepares to address the media regarding a failed drug test at The LA Hotel Downtown. Photograph: Kevork Djansezian/Getty Images. Maria Sharapova tested positive for......
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Sensex Opens in Green; Realty Sector Up by 2.4%

Posted by Equitymaster Stock markets in Asia are mixed today following the widely-expected results of the first round of presidential elections in... ...

http://feeds.equitymaster.com/~r/TodaysMarket/~3/VHhrmu-C6xs/tm.asp
Strides Shasun's Cuddalore plant completes USFDA inspection

Drug firm Strides Shasun today said its Cuddalore facility in Tamil Nadu has successfully completed inspection by the US health regulator. The... ...

http://www.business-standard.com/article/pti-stories/strides-shasun-s-cuddalore-plant-completes-usfda-inspection-117042400808_1.html
Sun Pharma's Dadra facility receives 11 USFDA observations after inspection

Drug major Sun Pharmaceutical Industries has received 11 observations from the US health regulator after inspection of its Dadra facility. The... ...

http://www.business-standard.com/article/companies/usfda-issues-11-observations-post-inspection-at-sun-pharma-s-dadra-facility-117042200624_1.html
company

SEOUL (Reuters) - South Korea's Samsung Bioepis Co Ltd said on Saturday the U.S. Food and Drug Administration approved its copy of Johnson &... ...

http://feeds.reuters.com/~r/reuters/INhealth/~3/kaRBC_6qLcQ/us-samsung-bioepis-approval-usa-idINKBN17N2LQ
Sensex, Nifty shed about 0.3% after lackluster sessions

Concerns about geopolitical tensions, weakness in global markets and caution ahead of key results rendered price movements quite sluggish in the... ...

http://www.sify.com/finance/weekly-wrap-sensex-nifty-shed-about-03-after-lackluster-sessions-news-sensex-rewlC3faagiag.html

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