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General Electric, Siemens Healthcare USA and Philips Healthcare

Apr 2011
An article in the February 2011 issue of the Journal of the American College of Radiology provides a road map for imaging manufacturers to navigate the increasingly complex US regulatory and reimbursement environment. “Evidence Requirements for Innovative Imaging Devices: From Concept to Adoption” addresses the five phases of an imaging procedure’s life cycle and the distinct clinical evidence needs for each phase. It examines the design, regulatory clearance and approval, early adoption, reimbursement and full clinical adoption of imaging technology. The article is co-authored by Richard Frank, vice president of global clinical strategy and policy at General Electric; Donald W. Rucker, chief medical officer of Siemens Healthcare USA; Michael A. Ferguson, global director of clinical outcomes and translational research at Philips Healthcare; and Terry J. Sweeney, senior vice president of corporate quality and regulatory affairs at Philips Healthcare.

BiophotonicsBusinessDonald W. RuckerGeneral Electricimagingimaging roadmapmedical device adoptionmedical imagingmedical reimbursementsmedical screening recommendationsMichael A. FergusonPhilips HealthcareRapidScanregulationsRichard FrankSiemens Healthcare USATerry J. Sweeney

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