Regulation
Views on the rules and regulations that govern medical technologies.
Posted on 15.10.2012
Eucomed: proposed overhaul of EU reg system mostly positive with one caveat
By John Brennan, Director Regulations and Industrial Policy
Posted on 18.09.2012
Wedding bells are ringing for the proposal of new IVD regulation
By Jesús Rueda Rodríguez, Director International Affairs MedTech Europe
Posted on 31.08.2012
Policy and regulation for innovation in mHealth
By Jeanine Vos, Executive Director, Mobile Health at GSMA
Posted on 25.07.2012
The impact of WEEE2 on the medical devices industry
By Andy Vaughan, Eucomed Environment Consultant
Posted on 09.07.2012
How the approval process of medical devices works in Europe
By John Brennan, Director Regulations and Industrial Policy
Posted on 02.07.2012
Toward the best possible solution in EU medical device labelling
By Merlin Rietschel, Manager Regulatory & Technical Affairs, Eucomed
Posted on 19.06.2012
Why PMA is a step backwards in the approval approach for medical technology
By John Brennan, Director Regulations and Industrial Policy
Posted on 09.05.2012
So where are we again on the Revision of the MDD?
By John Brennan, Director Regulations and Industrial Policy
Posted on 12.04.2012
Standalone software: objects in the regulatory mirror may appear simpler than they are
By Erik Vollebregt, Life Sciences and IP Lawyer, and Founding Partner Axon Lawyers
Posted on 28.03.2012
Centralised procurement – a blessing or a curse?
By Lotte M.G. Steuten, Assistant Professor, Universiteit Twente
Posted on 13.03.2012
Patient safety through smart regulation – A shared commitment of Europe’s medtech industry
By Luciano Cattani, Former Chief Executive of Eucomed
Posted on 11.01.2012
How should the EU regulatory framework change because of the PIP incidents?
By John Brennan, Director Regulations and Industrial Policy

