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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......

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......

Available now: A 'female Viagra', but it comes with a warning

The first drug to treat low sexual desire in premenopausal women, dubbed "female Viagra", has been approved in the United States, but with a warning about potentially dangerous side effects such as......

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......

FDA raises concern over US unit: Wockhardt

The US Food and Drug Administration (FDA) has expressed concerns over production processes at the US unit of Wockhardt Ltd, a senior executive said, possibly adding to a spate of regulatory......
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Amgen files for U.S. approval of biosimilar to Humira

By By | Reuters By Bill Berkrot (Reuters) - Amgen Inc on Wednesday said it filed with U.S. health regulators seeking approval to sell its... ...
Amgen's First Biosimilar Biologics License Application For ABP 501 Submitted To U.S. Food And Drug Administration

From the Wires Supported by Phase 3 Studies in Moderate-to-Severe Plaque Psoriasis and Moderate-to-Severe Rheumatoid Arthritis Nov. 25, 2015... ...

Hyderabad : In the most damaging observation against Dr Reddy's Laboratories (DRL), the US Food and Drug Administration (FDA) has accused the... ...
Sandoz gets FDA rap over documentation at plants

The US Food and Drugs Administration (FDA) has issued a warning letter to Sandoz, the generic drug division of Novartis, over the lack of proper... ...
FDA comes down heavily on Dr. Reddy's Lab

Significant deviations from current GMP for manufacture of APIs at two facilities and violations of CGMP regulations for finished pharmaceuticals... ...

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