The management systems community
14th Jul 2011
ARAMARK Healthcare, a leading provider of hospital support services, announced today that its European service business, Medical Equipment Solutions & Applications (MESA), has been certified to ISO 13485 by Lloyd’s Register Quality Assurance (LRQA).
18th Apr 2008 by Simon Emeny
Changes on the way for Medical Device conformity
The Medical Devices Directive (MDD) 93/42/EEC is well established. As is common with the EU, they decided that it couldn’t be left alone and instituted a review on its functioning. In summary, the conclusions were that the existing legal framework is appropriate, but that its implementation could be improved, including further regulatory clarification.
Event: 14th Feb 2008 – 15th Feb 2008
Country: Switzerland City: Lausanne Event website & Booking:www.medtechinvesting.com THE SIXTH MEDTECH INVESTING EUROPE CONFERENCE -LAUSANNE, SWITZERLAND, The premier European event, bringing together Med tech investors and innovators. If you are interested in investing in the med tech industry, or are a med tech company looking to find an investor, you cannot afford to miss Campden [...]
21st Jan 2008
The Consumer and Industrial Goods Directorate of the Malta Standards Authority, within the Ministry for Competitiveness and Communications, said it has closely followed and participated in the discussions at European level on the revision of the medical devices directives, a recent article in the Malta Independant Online reports.
15th Jan 2008
Research and Markets (http://www.researchandmarkets.com/reports/c79408) has announced the addition of EU Pricing and Reimbursement for Medical Devices and Diagnostics 2006 Report to their offering.
15th Jan 2008
The fundamental ethos and creativity of cancer research is threatened by too much management and excessive regulation, says a Keynote Comment in The Lancet Oncology, January 2008 issue. The Comment also adds that there is a serious lack of regulation harmonization between countries, a recent blog reports.
8th Jan 2008
Regulations controlling the manufacturing, marketing and usage of medical devices in the EU are forcing manufacturers to incorporate language translation. Read the full blog by Shy Avni, posted 8th january 2008.
18th Dec 2007
Don’t get too comfortable with your European Union (EU) Restriction of Hazardous Substances (ROHS) standing, as the directive is set to be adjusted in 2008 to reflect additional substances and changes to exemptions, a recent article reports.
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