The European Commission's public consultation on proposed revisions to the In Vitro Diagnostics Directive (98/79/EC) contains a section on "conditional CE marking" that has caught the attention of European medtech industry association Eucomed. John Brennan, Eucomed's director ...
Clinica
"Conditional CE marking" - a new concept in device innovation?
01 July 2010
Karen Finn
Not a subscriber ? Request a FREE Trial
Subscribe to Clinica
RELATED CONTENT
NEWS
Clinica News
- High-ranking EU Commission officials give latest update on device directive recast text
- EU IVD Directive: huge majority wants greater NB involvement
- Latest EU directive revision text: unannounced notified body visits and public access to their decisions in line
- Immediate improvements sought in EU-wide surveillance of medical devices post-PIP
Other Informa News
Features & Analysis
Other Informa Analysis
EVENTS
19 March 2012
Montreux Convention and Music Centre, Switzerland
