A centralised system for managing clinical trials in the EU and EEA, with publicly available information on clinical trials granted or refused permission via the system
Used by pharmaceutical companies to submit regulatory information concerning marketing authorisations applications to the national competent authorities and EMA
Used by pharmaceutical companies and national competent authorities to gather information about medicine supply and demand in the European Union (EU) and European Economic Area (EEA)
Helps regulators, pharmaceutical companies, and researchers in identifying the most suitable data sources to address specific research questions. Researchers also use it to register their observational studies.
Used by pharmaceutical companies for handling product-related scientific and regulatory procedures with EMA, with certain information accessible to all visitors