In 2017, the European Commission published a report regarding the possible improvements for product information texts used for human medicinal products. The improvements aim to facilitate the safe and effective use of medicinal products. Klaus Menges, Stan van Belkum, Jennie May and Peter Leister at PharmaLex show that as a result of the report, the European Medicines Agency (EMA) and the national heads of medicines agencies (HMAs) have agreed on a project to implement structured electronic ePI.