EMA Releases Updated Electronic Forms for Drug Marketing Applications

The European Medicines Agency (EMA) has issued updated versions of its interactive PDF electronic application forms (eAFs) for human marketing authorization applications. These Version 1.28.0.0 forms will become mandatory for new Centralized Procedure applications to EMA starting July 28, 2026. National Competent Authorities will also require these updated forms for various national and mutual recognition procedures from September 1, 2026.