We improved how this search looks for keywords. We also adjusted search filters. For details, see Website outages and upgrades. You can also download medicine data as published on this website in table format or check our search tips for help.
To fetch data from this website via automated systems, please use our JSON data files
Search results (155)
The European Medicines Agency (EMA) makes upgrades to this website from time to time, to improve user experience. During these upgrades, the website is unavailable for a short period of time, outside of EMA working hours. This page lists when we are planning the next outage and the main improvements made.
The European Medicines Agency (EMA) provides guidance and training materials to help stakeholders of the European Shortages Monitoring Platform (ESMP) adopt and use the platform. EMA also organises events to support them and facilitate their involvement in the platform’s development.
These questions and answers (Q&As) provide an overview of the European Medicines Agency's (EMA) advice on issues that are typically addressed in discussions or meetings with marketing authorisation holders in the application phase.
The Union Product Database (UPD) serves as a single source of information on all authorised veterinary medicines and their availability in European Union (EU) and European Economic Area (EEA) Member States. The European Medicines Agency (EMA) set up and maintains the veterinary medicines information website and the Union Product Database, in...
The staff and experts of the European Medicines Agency (EMA) publish articles on the Agency's scientific activities in scientific publications, such as journals or textbooks.
Each month, the European Medicines Agency's (EMA) publishes an updated list of medicines for human use currently under evaluation by EMA’s Committee for Medicinal Products for Human Use (CHMP) to obtain a marketing authorisation in the European Union (EU).