Greatbatch Scoops Up Micro Power for $60M Cash - Dec. 14, 2011

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Wednesday, December 14, 2011  |   |   |   |  The Master of Science (MS) in Medical Product Development Management (MPDM) at San Jose State University is a comprehensive, master's degree program and can be completed in either 2 or 3 years. The emphasis of the program is on the management of products undergoing clinical research and clinical development, i.e. clinical trial stages I, II, III and IV or other testing as required by the Federal Food and Drug Administration (FDA) or international regulatory authorities. The curriculum includes customized courses from the Colleges of Science and Business, and was designed in consultation with biomedical industry employers in the greater San Francisco Bay area. The MPDM program continues to have interaction with the industry and provides expert industry speakers in the classroom, in order to present the latest advancements to students. Please click here for more information.   •  Greatbatch, Inc. (GB) Scoops Up Micro Power Electronics for $60 Million Cash More... •  FDA Approves InfraScan Inc.'s Hand-Held Brain Bleed Detector More... •  Doctor's Medical Device Gets Quick FDA Approval More... •  Intuitive Surgical, Inc. (ISRG)'s Surgical Robot Accessory Gains FDA Clearance More... •  FDA Issues Warning Letters for Misleading Advertising of Allergan Inc. (AGN)'s Lap-Band More... More Top News SPIE: BiOS Exhibition 2012 January 21 - January 22, 2011 Moscone Convention Center San Francisco, California U.S.A. SPIE BiOS Exhibition, is the world's largest and most prestigious international biomedical optics and imaging conference & exhibition, encompassing clinical, translational, and fundamental R&D. BiOS provides you with a premier technical forum for reporting your achievements and learning about the latest clinical and technical advances. 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Act as SME for all products as they relate to product development including but not limited to Design control management and transfer process, Device history management, Change control, Verification, Validation, Optimization testing and Stability studies, and translation of technical information. • Genetown (Billerica, Massachusetts) Volcano Corporation Senior Quality Design Assurance Engineer Bring your expertise and participate in: Daily interaction with your R&D Engineering peer group. Design controls (21CFR820.30) and product realization (ISO13485) compliance activities DHF, Tech File, Design Dossier documentation and Design Risk Management activities. • Biotech Bay (Santa Clara, California) Abbott Senoir R&D Engineer - Stent Designer Responsible for providing mechanical engineering support in the creation and the development of new medical device products (invasive and non-invasive). • Rocky Bio (Salt Lake City, Utah) Watson Pharmaceuticals, Inc. 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