Abbott announced that FDA approved the XIENCE V Everolimus Eluting Coronary Stent System for the treatment of coronary artery disease. XIENCE V is the only drug eluting stent to have demonstrated superiority over Boston Scientific's TAXUS paclitaxel-eluting coronary stent system
Hansen Medical has received the FDA 510(k) clearance to market the CoHesion 3D visualization module for use in complex electrophysiology mapping procedures.
Neovasc, formerly Medical Ventures, has changed its name and expanded product portfolio, as the company completed the acquisition of two vascular product development companies and the closing of an $8.3 million private financing.
Austria-based Nabriva Therapeutics, which is engaged in the discovery and development of antibacterial agents, has appointed George Golumbeski as CEO of the company.
Bayer HealthCare has announced that its consumer care division has achieved the necessary regulatory approvals to complete the acquisition of the western over-the-counter cough and cold portfolio of Topsun Science and Technology Qidong Gaitianli Pharmaceutical by Bayer Healthcare Company in
HD Medical has entered into a distribution agreement with BPL for the distribution of the company's first pipeline product, ViScope 100. The distribution agreement is valued at $10 million.
SkyePharma has announced that its third Phase III efficacy study evaluating Flutiform for the treatment of mild to moderate asthma in adolescent and adult patients has met its primary endpoints.
Jerini and Shire have reached a strategic agreement according to which Shire shall be obliged to make a voluntary public takeover offer to all shareholders of Jerini.
USHIFU, a provider of non-invasive high intensity focused ultrasound for prostate cancer, has acquired Focus Surgery, a manufacturer of the Sonablate 500, an image-guided acoustic ablation device.
Patheon has completed a shareholders agreement and a sales and marketing agreement with BSP Pharmaceuticals, a company focused on the development and manufacturing of cytotoxic pharmaceutical products.
ARYx Therapeutics has announced that Procter & Gamble Pharmaceuticals has utilized a one-time 30 day cancellation option linked to the completion of a Thorough QT study to end the collaboration agreement between the two companies.