Brussels, 24/06/2013 (Agence Europe) - On 21 June in Luxembourg, the Irish Presidency of the Council of the EU presented health ministers with two progress reports, one focusing on work on clinical trials of medicines for human use and the other on medical devices (for in vitro diagnosis).
On 17 July 2012, the European Commission adopted a draft regulation to boost clinical research in Europe by improving the lengthy and rather opaque authorisation process (see EUROPE 10657). In first...