EN PL

MHRA: EMA public consultation on functional specification for portal and database that will underpin the EU Clinical Trials Regulation

23.10.2014
One of the features of the EU Clinical Trials Regulation No 536/2014 is the creation of the EU portal and the EU database for clinical trials. The Regulation and systems infrastructure provided by the portal and database are intended to simplify and harmonise the submission, assessment and reporting of clinical trials.