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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......
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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
Conatus Announces Successful Top-Line Results From NAFLD/NASH Clinical Trial of Emricasan

- Conclusions Support Registration Strategy Including NASH Cirrhosis - - Detailed Data to be Presented in Late-Breaker Poster at EASL Meeting - SAN... ...

http://www.bizwireexpress.com/showstoryGNW.php?storyid=64879
Cardio3 BioSciences Reports 2014 Financial and Operating Results

Significant Progress Made in Building a Global Specialty Therapeutics Company Conference Call to be Held on 26 March 2015 at 2.00 p.m. CET / 9.00... ...

http://www.bizwireexpress.com/showstoryGNW.php?storyid=64867
Stryker Spine receives FDA Clearance for New Lumbar Plating System

Stryker Corporation's Spine Division announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the... ...

http://www.asianhhm.com/pressreleases/stryker-spine-receives-fda-clearance-for-new-lumbar-plating-system
La Jolla Pharma begins phase 3 trial of LJPC-501 in catecholamine-resistant hypotension

La Jolla Pharmaceutical Company, a leader in the development of innovative therapies intended to significantly improve outcomes in patients... ...

http://www.pharmabiz.com/NewsDetails.aspx?aid=87387&sid=2

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