The Heads of Medicines Agencies (HMA) in Europe has launched a trial to publish electronic product information (ePI) for human medicines across the European Union on a public Product Lifecycle Management Portal.
The HMA, which is made up of the heads of national authorities responsible for human and veterinary medicines in each country of the European Economic Area, has launched the trial together with the European Medicines Agency (EMA) and the European Commission (EC).
The trial will assess the feasibility of transitioning key regulatory documents, evaluated both nationally and at a European level, to an online electronic portal. The documents include the Summary of Product Characteristics (SmPC), product labeling, and the Package Leaflet (PL), which will be publicly available in the official languages of the relevant member states.
