Regulation
Views on the rules and regulations that govern medical technologies.
Posted on 01.07.2011
Standards: To infinity (well the next decade at least) and beyond
By Andy Vaughan, Eucomed Environment Consultant
Posted on 09.06.2011
Rethinking medical device manuals to save lives and trees
By John Brennan, Director Regulations and Industrial Policy
Posted on 07.06.2011
eHealth applications and websites developed by clinicians: there are rules for that!
By Erik Vollebregt, Life Sciences and IP Lawyer, and Founding Partner Axon Lawyers
Posted on 18.03.2011
Effective solutions to prevent 4.1 million healthcare associated infections in Europe
By John Bowis, Honorary President, Health First Europe
Posted on 03.03.2011
WEEE & RoHS: the dynamic duo that wants to keep people healthy
By Andy Vaughan, Eucomed Environment Consultant
Posted on 15.02.2011
The ‘New Approach’ – making standards even better
By Andy Vaughan, Eucomed Environment Consultant
Posted on 08.02.2011
Brussels starts healthy debate on Medical Device Recast
By John Brennan, Director Regulations and Industrial Policy
Posted on 10.01.2011
Panel-mania? The future of an advisory interpretation
By Aline Lautenberg, MedTech Europe, General Counsel - Director Legal & Compliance
Posted on 17.12.2010
You better watch out!
By John Brennan, Director Regulations and Industrial Policy
Posted on 18.11.2010
There’s a good future in (DG) Research
By John Brennan, Director Regulations and Industrial Policy
Posted on 21.10.2010
Can we move global harmonisation to the next level?
By John Wilkinson, Former Chief Executive of Eucomed
Posted on 07.09.2010
To Reuse or not to Reuse – that is the question (and with apologies to lovers of Shakespeare)
By John Brennan, Director Regulations and Industrial Policy

