10. November 2023 – The Heads of Medicines Agencies (HMA), the European Commission (EC) and the European Medicines Agency (EMA) have published for the first time electronic product information (ePI) for selected human medicines harmonised across the European Union (EU). The product information of a medicine includes its summary of product characteristics, labelling and package leaflet. These documents accompany every medicine authorised in the EU and explain how they should be prescribed and used.

For more information, see here.