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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 ...
 
08 July 2010
Maureen Kenny
German or Spanish physicists hoping for a career change involving a move to London at the end of the year and taking charge of the European Medicines Agency have had their hopes dashed. It turns out, not surprisingly, that the person who will ...
 
05 July 2010
As doctors in the US brace themselves for the 30 million new patients that the new healthcare reform law promises to channel into the system, a key mechanism for advancing their medical knowledge and performance is facing tumultuous times. Certified ...
14 May 2010
The implementation deadline of 21 March has gone by and new safety reporting requirements for clinical investigations are now in place throughout the European Union. As a result of the revisions made to the medical device directives by Directive ...
12 January 2010
There has been talk of allowing e-labelling in the European Union for years now, yet companies still have to supply their instructions for use in hard copy. The situation could – and should – change soon, says Joachim Wilke . The change that will ...
 
08 October 2009
Please give details of the major acts and directives governing trademarks. Trademarks are governed in Luxembourg by the: Benelux Convention on ...
08 October 2009
1) Which authority is responsible for overseeing the regulation of medical devices and diagnostics in Spain? Agencia Española del Medicamento, the ...
RAJ Devices News Roundup, July 2010
19 July 2010
 
 
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