Scrip
Clinica
RAJ
Scrip Clinical Research
Animal Pharm
Email ID
Password
Forgotten password?
Sign me in automatically next time
Advanced Search
Home
Product Sector
Regulatory Region
Pre-marketing Regulation
Post-marketing Regulation
Healthcare Systems
Legal
IP
|
Product Liability
|
Legal - IP
Loading IP ....
>> More Ip...
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
Counterfeits: Opportunities for MEDICRIME, Challenges for IMPACT
07 July 2010
Alan Chalmers reports that progress was made at a conference on the Council of Europe's proposed MEDICRIME convention, despite the controversy ...
Tackling Counterfeit Medical Devices in Turkey
17 May 2010
Bariş Kalaycı and Arda Özgil explain how companies can protect their products despite the lack of specific anti-counterfeiting legislation in Turkey. ...
Medical Device Counterfeiting - Still Very Much an Unknown
01 February 2010
Medical device counterfeiting clearly exists. Adrie de Bruijn , Claudette de Vries and Harm Hermsen report that while around the world authorities ...
>> 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
About Us
Getting Started
Free Trial
Subscribe
Advertise
Guidelines for Authors
Blog
EVENTS
