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• Watson confirms filing of ANDA for generic version of Lo Loestrin Fe with FDA Pharmaceutical Business Review The lawsuit was filed under the provisions of the Hatch-Waxman Act, resulting in a stay of final FDA approval of Watson's ANDA for up to 30 months from the date the plaintiff received notice of Watson's ANDA filing or until final resolution of the ... and more »

• Chelsea Therapeutics International Ltd. (NASDAQ:CHTP) Investor files Lawsuit ... Your-Story.org (press release) The plaintiff claims that Chelsea Therapeutics International Ltd knew that the drug was not fit for FDA approval and unlikely to obtain FDA approval due to serious health risks after at least 19 deaths during clinical trials. Then on February 13, 2012, ...

• No Obligation Defective Vaginal Mesh Lawsuit Legal Evaluation DigitalJournal.com (press release) According to the site the surgical mesh products used have been linked by the FDA to a number of possible complications including: "We have a uniquely experienced attorney who was a former nurse herself, available to women who would like to learn more ...

• Watson faces lawsuit over generic contraceptive PMLiVE Ireland-based pharma firm Warner Chilcott filed a lawsuit in the New Jersey District Court following Waton's filing of an abbreviated new drug application with the US Food and Drug Administration (FDA) ahead of the drug's patent expiration. and more »

• Owner of Utah gluten-free bakery sues Hatch Ventura County Star Orrin Hatch, claiming he has stymied funding for the FDA to enact gluten-free labeling regulations. Tim Lawson, in his lawsuit filed Thursday in US District Court in Salt Lake City, said the regulations are needed to help people afflicted with an ... and more »

• FDA rule clears medical devices without human testing OCRegister "The 510 (k) program is the weakest and most nonsensical program in the FDA." Dr. Melvin Silverstein, medical director of Hoag Breast Care Center and Kelly's surgeon, declined requests to be interviewed for this article, citing lawsuits against Hoag by ... and more »

• Rigrodsky & Long, P.A. Announces A Securities Fraud Class Action Lawsuit Has ... EON: Enhanced Online News (press release) The Company's principal product is Vancocin, an antibiotic which was approved by the FDA in intravenous form more than half a century ago under the name Vancomycin. The Complaint alleges that throughout the Class Period, defendants made materially ... and more »

• Utah gluten-free baker sues Hatch over FDA funding Salt Lake Tribune But Lawson's lawsuit said the FDA has failed to enact gluten-free labeling regulations, in part because Hatch has refused to use his influence to get funding for the agency. As a result, Lawson said people who are buying gluten-free products are ... and more »

• A Look Back at Accutane Side Effects Lawsuits Accutane Lawsuit Center - Injury Litigation News 24/7 When Accutane (isotretinoin) was first approved by the FDA as an anti-acne drug in 1982, it was seen as an effective solution for teens and adults suffering from the embarrassment of severe acne and problem skin that didn't respond to other treatments. and more »

• Groups drop lawsuit over food nanotechnology Capital Press (subscription) Plaintiffs in the case have agreed to drop the lawsuit because the FDA has formally responded to their petition, though the agency rejected some of their key proposals. In the 2006 petition, the International Center for Technology Assessment and ...

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