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Pharmaceutical

EU, US health officials team up to fight antimicrobial resistance

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Health officials from both sides of the Atlantic have been working together to tackle antimicrobial resistance under their joint Transatlantic Taskforce on Antimicrobial Resistance.
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Pfizer proposes $101 billion takeover to AstraZeneca, reports claim

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U.S. pharmaceutical company Pfizer has expressed interest in taking over Anglo-Swedish giant AstraZeneca for a total of $101 billion.
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New FDA import ban hits Indian drug-making industry

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The FDA's campaign against substandard pharmaceutical products manufactured in India is continuing with a new import ban, this time imposed on drugs produced at a Bangalore facility owned and operated by Canadian company Apotex Inc.
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FDA bans import of drugs from Sun Pharma's Gujarat facility

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The U.S. FDA has issued an import alert for Indian drug maker Sun Pharmaceuticals Ltd., banning the import of drug products manufactured at the company's facility in Gujarat.
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Indian pharmaceutical firms braced for effect from US drug supply market mergers

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The U.S. pharmaceutical supply chain is predicted to go through a stage of consolidation which will have an impact on the Indian drug manufacturing market, according to industry experts.
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US, Indian officials meet to discuss drug safety

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India and the United States have been locked in a regulatory conflict over generic pharmaceutical products distributed on the U.S. market.
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Mexico's Neolpharma opens R&D facility in Puerto Rico

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The Center for the Development and Innovation of Pharmaceutical Products, or Cediprof, will focus on research and experimentation of generic drugs.
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Another Ranbaxy facility lands on FDA blacklist

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The U.S. Food and Drug Administration (FDA) has added Ranbaxy's Toansa plant to the list of Indian facilities included on the consent decree dated January 2012.
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Israel's Teva to buy NuPathe for $144 million

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Pennsylvania-based NuPathe specializes in therapeutics for diseases of the central nervous system (CNS), including neurological and psychiatric disorders.
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US, European watchdogs join forces to regulate generic drugs

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The European Medicines Agency and the U.S. Food and Drug Administration have started a joint program for sharing information on bioequivalence studies required during the process of approval for generic drugs.
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