European legislation regulating the marketing authorisation of medical products states that results from clinical trials that do not meet the ethical requirements of Good Clinical Practice, cannot legally be used by an applicant to justify its application, irrespective of whether the trial was...

This Synthesis Report presents the main findings of the 2017 EMN Study Approaches to Unaccompanied Minors Following Status Determination in the EU plus Norway. The study covers the period 2014-2017, thereby following up on previous EMN research on unaccompanied minors. It may serve to inform...

The purpose of this report is to set out in brief form the law across the EU Member States, Bulgaria and Romania relating to discrimination on grounds of sex, sexual orientation, disability, religion and belief and age (the u0093relevant groundsu0094), to the extent that such discrimination...

Research infrastructures (RIs) are the most powerful means to foster cooperation on a pan-European scale and to provide efficient access to advanced methods and technologies for the scientific community.The existence, availability and easy access to leading research infrastructures is a key...