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Jun 11, 2026 · The European Medicines Agency (EMA) announced the publication of its 2025 Annual Report on June 11, 2026, 1 revealing a strong year of regulatory output across both human and veterinary medicines —along with significant advances in biosimilar policy, medicines availability, and the integration of artificial intelligence into agency operations About the Generic Medicines Group The Generic Medicines Group is a sector group of Medicines for Europe , representing the generic medicines developers and manufacturers, which provide high-quality cost-competitive medicines to millions of patients in Europe and around the world Over 400 manufacturing and research & development sites across Europe produce your essential medicines , employ over Medicines For Europe (formerly EGA) represents the European generic, biosimilar and valued added pharmaceutical industries The European Medicines Agency (EMA) is responsible for the scientific evaluation of centralised marketing authorisation applications EMA's opinion refers to its scientific recommendation, upon which the European Commission bases its legal decision to grant an EU -wide marketing authorisation 1 day ago · The European Medicines Agency (EMA) has implemented a strategy to accelerate drug approvals in the EU Learn more about their initiatives and how they are streamlining the process for faster Jun 9, 2026 · The European Parliament and the Council reached a provisional agreement on May 12, 2026, on the Critical Medicines Act (“CMA”), a separate regulation designed to shore up the availability and Apr 27, 2026 · The reform introduces a number of targeted changes to marketing authorisation applications and related regulatory processes, aimed at increasing efficiency and strengthening environmental oversight, while at the same time reinforcing the resilience of the EU medicines supply chain
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