Regulation
Views on the rules and regulations that govern medical technologies.
Posted on 13.04.2016
Finding solutions to notified bodies challenge is crucial
By Serge Bernasconi, Chief Executive Officer, MedTech Europe
Posted on 10.11.2015
During Trilogue, IVD and MD files should be treated on their own merits
By Serge Bernasconi, Chief Executive Officer, MedTech Europe
Posted on 22.10.2015
What’s with all the unnecessary complexity on the medical device revision?
By Serge Bernasconi, Chief Executive Officer, MedTech Europe
Posted on 26.05.2015
Why the Parliament report on safer healthcare matters to wound care
By Paul Trueman, Chair, Eucomed Advanced Wound Care Sector Group; Vice-President of Market Access Smith & Nephew
Posted on 18.03.2015
New EP, new Commission, another Presidency – Where does the IVD legislation stand?
By Jesús Rueda Rodríguez, Director International Affairs MedTech Europe
Posted on 30.09.2014
Innovation outpacing EU regulation: the case for medical 3D printing
By Wilfried Vancraen, Chief Executive Officer
Posted on 22.05.2014
Let’s close clinical loopholes for devices and not just ‘wallpaper over the cracks’
By Serge Bernasconi, Chief Executive Officer, MedTech Europe
Posted on 28.04.2014
Clinical Evidence “for In Vitro Diagnostics” should be exactly that: “for IVDs”
By Serge Bernasconi, Chief Executive Officer, MedTech Europe
Posted on 26.02.2014
Where are we again on the MDD and IVDD?
By Serge Bernasconi, Chief Executive Officer, MedTech Europe
Posted on 29.01.2014
“Harmonised” data protection in the EU: a new barrier to patient access to medtech?
By Chantal Vets, Senior Legal Director, Medtronic
Posted on 27.11.2013
Hats off to policymakers for encouraging multidisciplinary wound care
By Paul Trueman, Chair, Eucomed Advanced Wound Care Sector Group; Vice-President of Market Access Smith & Nephew

