C221532Level 6
EudraVigilance
**Semantic type:** Intellectual Product
**Definition:** The system for managing and analyzing information on suspected adverse reactions to medicines which have been authorized or being studied in clinical trials in the European Economic Area (EEA). The European Medicines Agency (EMA) operates the system on behalf of the European Union (EU) medicines regulatory network. (EMA)
**Synonyms:** - EUDRAVIGILANCE
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