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Procter & Gamble Pharmaceuticals Launches Asacol(R) HD (mesalamine) Delayed-Release Tablets
Procter & Gamble Pharmaceuticals (P&GP) announced the availability of Asacol HD (mesalamine) delayed-release tablets, which are indicated for the treatment of moderately active ulcerative colitis (UC), a form of inflammatory bowel disease. UC involves inflammation of the lining of the colon and rectum and is typically characterized by flares followed by periods of remission. Moderately active UC is characterized by tougher symptoms than mildly active UC. Asacol HD is proven to help treat these tougher flares of moderately active UC. Asacol HD was approved by the U.S. Food and Drug Administration (FDA) based on evaluations from the ASCEND studies [Assessing the Safety and Clinical Efficacy of a New Dose of 5-ASA (4.8 g/day 800 mg tablet)].
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Doctors Welcome Review Of Mental Health Services
The BMA welcomed the publication of Audit Scotland"s Overview of mental health services but warned that psychiatry continues to be the "Cinderella specialty" when it came to funding.
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American Lung Association Applauds EPA For Taking Critical Steps To Protect Public Health From Global Shipping Pollution
Statement of Captain Charles D. Connor, U.S. Navy (Ret.), American Lung Association President and CEO:
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Canada And European Communities End World Trade Organization Biotech Dispute

Canada and the European Communities announced the end of a six-year World Trade Organization (WTO) dispute regarding the approval and marketing of biotechnology products. Sharon Bomer Lauritsen, Executive Vice President, Food and Agriculture for the Biotechnology Industry Organization (BIO), issued the following statement in response: "While it is a good sign to see that Canadian canola growers have gained some access for their exports, the European Union"s approval system for agricultural biotechnology products continues to be broken. It is plagued by political interference, undue delay and member state prohibitions. "There are now 70 products awaiting approvals - compared to 40 last year. There are no new cultivation approvals - in fact - France and Germany have imposed cultivation bans within the past two years. In addition, biotech corn is still not moving into the EU. "This situation impedes U.S. trade, despite the well-documented safety of agricultural biotechnology which has produced real results towards increasing crop yields, reducing production inputs and enhancing environmental sustainability. "The EU"s non-functioning biotech approval process has blocked U.S. agricultural exports to the detriment of American farmers and agribusiness, but also has prevented European farmers from benefiting from modern technologies that are used in 25 countries by 13.3 million farmers around the world. "Trade problems will continue to exist until Europe has a science-based, timely and predictable approval process, which could be achieved if the EU simply followed its own laws and regulations. "We urge the European Commission to normalize trade of products produced through biotechnology in a timely and science-based manner." BIO


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