Regulation
Views on the rules and regulations that govern medical technologies.
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
Posted on 03.11.2011
What did Europe ever do for us?
By John Wilkinson, Former Chief Executive of Eucomed
Posted on 12.10.2011
Safeguarding Europe’s healthcare for the future together
By John Wilkinson, Former Chief Executive of Eucomed
Posted on 17.08.2011
My thoughts on mixing HTA with regulation? The writing’s on my wall…
By Victoria Malakhova, Former Eucomed Director Economic Affairs

