Regulatory: Page 34

European radiology mobilizes to stave off MRI safety rules
By Brian Casey
VIENNA - A number of European academic societies, including the European Society of Radiology (ESR), have formed a coalition to try to prevent the adoption of safety rules set to go into effect in 2008 that could severely limit the types of MRI studies that can be conducted in the European Union. Called the Alliance for MRI, the coalition was launched here today at the European Congress of Radiology (ECR).
March 8, 2007
ART lands CE Mark
By AuntMinnieEurope.com staff writers
Canadian optical molecular imaging developer ART Advanced Research Technologies has received the European CE Mark for its SoftScan optical breast imaging device.
February 7, 2007
Advanced Magnetics, Guerbet file for European clearance of Combidex
By AuntMinnieEurope.com staff writers
MRI contrast developer Advanced Magnetics said that its European partner Guerbet has filed a marketing authorization application (MAA) with the European Agency for the Evaluation of Medicinal Products (EMEA) for its Combidex functional MRI agent.
December 5, 2006
NeuroLogica nets CE Mark
By AuntMinnieEurope.com staff writers
Mobile CT developer NeuroLogica has received the European CE Mark for its CereTom portable CT scanner.
October 8, 2006
eRad scores CE Mark
By AuntMinnieEurope.com staff writers
PACS firm eRad has received the CE Mark for its PACS offering.
September 27, 2006
IMS gets Canadian clearance for Giotto
By AuntMinnieEurope.com staff writers
Italian x-ray and mammography systems developer Internazionale Medico Scientifica (IMS) has received clearance to market its Giotto Image MR-CA mammography unit in Canada.
July 26, 2006
Hologic receives EUREF approval
By AuntMinnieEurope.com staff writers
Hologic has received Type Approval from the European Reference Organization for Quality Assured Breast Screening and Diagnostic Services (EUREF) for its Selenia digital mammography and SecurView systems.
July 19, 2006
Matrox shipping RoHS boards
By AuntMinnieEurope.com staff writers
Medical display controller board developer Matrox Graphics reported that four of its display controller board series are compliant with the European Parliament and the Council of the European Union directive on the restriction of the use of certain hazardous substances (RoHS) in electrical and electronic equipment.
July 17, 2006
St. Jude Medical gets CE Mark
By AuntMinnieEurope.com staff writers
Medical device manufacturer St. Jude Medical of St. Paul, MN, reported that it has received European CE Mark approval for its QuickOpt timing cycle optimization application.
June 15, 2006
Medtronic nets French reimbursement approval
By AuntMinnieEurope.com staff writers
Interventional technology firm Medtronic said it has received reimbursement approval in France for its Endeavor drug-eluting coronary stent system.
June 11, 2006
Boston Scientific gets EC nod for added Liberte uses
By AuntMinnieEurope.com staff writers
Interventional device firm Boston Scientific reported that it has received indication extensions to the European CE Mark for its Taxus Liberte paclitaxel-eluting coronary stent system.
May 15, 2006
IDev gets CE Mark for stent
By AuntMinnieEurope.com staff writers
Peripheral vascular disease treatment developer IDev has received the CE Mark for its nitinol stent in Europe.
May 3, 2006
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