European Medical Agency (EMA)

The European Medicines Agency (EMA) is a regulatory body that evaluates and supervises medicines and vaccines across Europe. Its main role is to assess the safety, effectiveness, and quality of medical products before they are approved for use, ensuring they meet rigorous standards. The EMA also monitors medicines after approval to identify any risks or side effects. By coordinating with national agencies in European countries, it helps facilitate access to safe and effective treatments for patients across the region.