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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......

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......

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......

USFDA raises concern over drug production process at Cadila

Sources say FDA letter over product and not entire facilityThe US Food and Drug Administration (FDA) has expressed concerns over the manufacturing process of at least one product at drugmaker......
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RIP Ranbaxy

Senior Editor P.B. Jayakumar Soon Ranbaxy Laboratories will cease to exist as the company is merging with Sun Pharmaceutical Industries. Such... ...

http://businesstoday.intoday.in/story/ranbaxy-laboratories-merger-final-with-sun-pharma-to-delist/1/217365.html
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
Advaxis to Present at the Jefferies Immuno-Oncology Summit

(GLOBE NEWSWIRE) -- Advaxis, Inc. (Nasdaq:ADXS), a clinical-stage biotechnology company developing cancer immunotherapies, announced today that it... ...

http://www.bizwireexpress.com/showstoryGNW.php?storyid=64877
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

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