Towards electronic product information for EU medicines

November 21, 2018 – EMA, the Heads of Medicines Agencies (HMA) and the European Commission (EC) are organising a workshop on 28 November 2018 in London to agree with various stakeholders on common European Union key principles to pave the way for implementing electronic product information (ePI) in the EU. The product information (PI) of a medicine in the EU includes the package leaflet for patients and the summary of product characteristics … (leggi tutto)