Medical Device Alert – Finalised texts of the new EU Regulations on medical devices and in-vitro diagnostic medical devices are out February 24, 2017
New Belgian Sunshine Requirements applicable to all pharmaceutical and medical devices from 1 January 2017 February 8, 2017
France imposes an extra notification obligation on Class III and implantable medical devices manufacturers January 30, 2017
Revisions to Clinical Data Publication Guidance extends scope of EMA disclosure power to clinical data submitted before 1 January 2015 December 20, 2016