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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 ...
INTERVIEW
In the industry's words
02 July 2010
On tenterhooks over the US Food and Drug Administration's reform of the 510(k) review process, the US medical technology industry is warning that the ...
LATEST FEATURES
Implications of the UK Bribery Act
06 July 2010
Tony Lewis and Alison Dennis urge medical device companies to review their compliance policies ahead of the Act's entry into force. The UK Bribery ...
In the industry's words
02 July 2010
On tenterhooks over the US Food and Drug Administration's reform of the 510(k) review process, the US medical technology industry is warning that the ...
Regulating Medical Devices in Switzerland
14 January 2010
Margit Widmann and Peter Studer of Swissmedic’s medical devices division talk to Karen Finn about how Switzerland’s unique role as an EU MRA contract ...
>> More Latest Features...
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 ...
>> More Latest Country Profiles...
MULTIMEDIA
RAJ Devices News Roundup, July 2010
19 July 2010
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