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Healthcare Systems - Policy
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EXPERT VIEW
In praise of the CE marking, but medtech's worst fear is still alive
06 July 2010
Ashley Yeo
The European Medicines Agency review meeting in London on 30 June passed with scarcely a mention of devices and diagnostics. This was perhaps as expected, given that the meeting, held to examine the outcomes of the assessment of Ernst & Young's ...
LATEST FEATURES
Globalisation Drives Device Regulation
13 January 2010
Karen Finn highlights the key events that shaped global medical device regulatory affairs in 2009. Many regulatory developments in the medical ...
Implementing the New EU Legislation on Advanced Therapy Medicinal Products
24 April 2009
The large number of people who attended the European Medicines Agency ’s first workshop on advanced therapy medicinal products reflects the interest ...
Nanotechnology and the European Product Liability Directive
02 April 2009
A key area for the development of nanotechnology is in medicines and medical devices. The application of nanotechnology to health, sometimes referred ...
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LATEST COUNTRY PROFILES
Trademarks Briefing (Devices) - Luxembourg
08 October 2009
Please give details of the major acts and directives governing trademarks. Trademarks are governed in Luxembourg by the: Benelux Convention on ...
Regulation of Medical Devices Briefing - Spain
08 October 2009
1) Which authority is responsible for overseeing the regulation of medical devices and diagnostics in Spain? Agencia Española del Medicamento, the ...
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MULTIMEDIA
RAJ Devices News Roundup, July 2010
19 July 2010
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