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Postmarketing Regulation - Promotion
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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
Electronic Cigarettes - Common Concerns but Not Much Regulatory Consensus (Update)
30 November 2009
Peter Charlish looks at the regulation of “e-cigarettes” and finds they can be drugs, devices, neither or both. Unless it is very tightly drawn up, ...
Stakeholders Deliberate on Developing US Social Media Guidance
27 November 2009
Jeanette Marchant reports on discussions at the US Food and Drug Administration public hearing on how drug and medical device companies should use ...
Off-Label Promotion in the US: Protecting Your Company and Employees
13 October 2009
Retta M Riordan examines manufacturers’ settlements with the government and provides advice on how to avoid prosecution. “Pfizer to pay record $2.3 ...
>> 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 ...
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MULTIMEDIA
RAJ Devices News Roundup, July 2010
19 July 2010
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