Regulatory: Page 28

IAEA creates database to record R/F incidents
By AuntMinnieEurope.com staff writers
The International Atomic Energy Agency (IAEA) has established an international database to report high radiation exposure incidents and adverse events relating to fluoroscopically guided diagnostic and interventional procedures.
May 5, 2011
InfraReDx gets CE Mark for IVUS system
By AuntMinnieEurope.com staff writers
Coronary imaging developer InfraReDx has received CE Mark approval to begin commercialization of its LipiScan intravascular ultrasound (IVUS) coronary imaging system throughout Europe.
April 20, 2011
Sectra nets Russian OK for digital mammo
By AuntMinnieEurope.com staff writers
PACS and digital mammography developer Sectra has received clearance to market its Sectra MicroDose Mammography system in Russia.
April 18, 2011
St. Jude to bring Accent MRI pacemaker to Europe
By AuntMinnieEurope.com staff writers
Cardiac technology developer St. Jude Medical has received the European CE Mark for its Accent MRI pacemaker and Tendril MRI lead.
April 17, 2011
Lansley says sorry to nurses over health reforms
By Reuters Health
LONDON(Reuters) - Health Secretary Andrew Lansley apologized for the poor communication of his health reforms and said changes would be made to draft legislation after nurses passed a vote of no confidence in him.
April 13, 2011
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U.K. coalition puts brake on NHS reform
By Reuters Health
LONDON (Reuters) - Britain's coalition government said on Monday it would slow the pace of a radical shake up of the state-funded National Health Service (NHS), reflecting growing unease over the issue within the ruling alliance.
April 4, 2011
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U.K. coalition puts brake on NHS reform
By Reuters Health
LONDON (Reuters) - Britain's coalition government said on Monday it would slow the pace of a radical shake up of the state-funded National Health Service (NHS), reflecting growing unease over the issue within the ruling alliance.
April 3, 2011
U.K. report criticizes equipment purchasing at NHS trusts
By Rebekah Moan
The U.K.'s National Health Service (NHS) is leaving trusts to their own devices, literally and figuratively, when it comes to purchasing medical imaging equipment, according to a report published by the National Audit Office on 30 March.
March 30, 2011
Regulatory group ejects industry members
By AuntMinnieEurope.com staff writers
A regulatory group charged with harmonizing device regulations in countries around the world has decided to continue on without industry participation. The Global Harmonization Task Force earlier this month told its partners in the device industry that they would no longer be allowed to participate in task force activities.
March 21, 2011
Covidien gets nod for South African Mo-99
By AuntMinnieEurope.com staff writers
Covidien has received approval from the U.S. Food and Drug Administration to use molybdenum-99 (Mo-99) from a South African firm for the production of technetium-99m generators at its Maryland Heights, MO, manufacturing facility.
March 13, 2011
'Guinea pig' remark spurs U.S., EU device spat
By Reuters Health
WASHINGTON (Reuters) - A trans-Atlantic spat has erupted after a top U.S. official suggested European patients may be "guinea pigs" for medical devices with less government oversight.
February 28, 2011
2011 02 09 16 36 57 148 Reuterslogo
Philips nets CE Mark for PET/MRI
By AuntMinnieEurope.com staff writers
Philips Healthcare has received the CE Mark for its whole-body Ingenuity TF PET/MRI system.
January 24, 2011
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