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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......

Gutkha worth over Rs 7 lakh seized in Maharashtra

The Maharashtra Food and Drug Administration seized gutkha worth over Rs 7 lakh from various parts of the state over the last two days in an effort to enforce the ban on gutkha sales."So far we......

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......

Sklamberg on challenges the US drug regulator faces globally

The US Food and Drug Administration (FDA) says it does not follow an India agenda. Howard R Sklamberg (below left), deputy commissioner, global regulatory operations and policy, FDA, tells Digbijay......

Ranbaxy loses exclusivity on heartburn drug in US

  Drug maker Ranbaxy’s troubles with the US Food and Drug Administration (FDA) continue, with the American regulator allowing Israel-based Teva Pharma to launch the generic of Nexium, a......

Ranbaxy sues US FDA for revoking drug approvals

FDA had cancelled Ranbaxy's approvals to launch generic Nexium, Valcyte Ranbaxy Laboratories Ltd has sued the US Food and Drug Administration (FDA) for revoking approvals granted to the firm to......

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......

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......
  Web results for Food Drug Administration
Micropacemaker to treat foetus with heart block

In a first, researchers have designed a fully implantable micropacemaker for use in a foetus with complete heart block.Reported in the journal... ...

http://www.prokerala.com/news/articles/a539226.html
In swansong, FDA chief defends drug approval process

WASHINGTON (Reuters) - In her final speech after six years as commissioner of the U.S. Food and Drug Administration, Dr. Margaret Hamburg defended... ...

http://feeds.reuters.com/~r/reuters/INhealth/~3/JSpatbtkbtM/us-fda-commissioner-speech-idINKBN0MO00V20150328
FDA rejects Adamis injection for treating acute allergies

(Reuters) - The United States Food and Drug Administration rejected Adamis Pharmaceuticals Corp's injection for treating severe allergic reactions,... ...

http://feeds.reuters.com/~r/reuters/INhealth/~3/HQ_TK1HM1C8/us-adamis-pharma-fda-idINKBN0MN2M420150327
FDA seizes artificially ripened mangoes

The Food and Drug Administration (FDA) officials on Friday seized mango consignments worth over Rs 3 lakh from two city traders, who used calcium... ...

http://timesofindia.feedsportal.com/c/33039/f/533982/s/44df3718/sc/26/l/0Ltimesofindia0Bindiatimes0N0Ccity0Cpune0CFDA0Eseizes0Eartificially0Eripened0Emangoes0Carticleshow0C46720A7410Bcms/story01.htm
Galena Biopharma Expands Patient Population in NeuVax(TM) (nelipepimut-S) and trastuzumab Phase 2b Combination Clinical Trial in HER2 1+/2+ Patients

Enrollment Eligibility Expanded to Include Human Leukocyte Antigen A24 or A26 Positive Patients PORTLAND, Ore., March 26, 2015 (GLOBE NEWSWIRE)... ...

http://www.bizwireexpress.com/showstoryGNW.php?storyid=64882

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