Better safety monitoring for patients across Europe

23 November 2017

The European Medicines Agency has launched a new and improved version of EudraVigilance, the European information system of suspected adverse reactions to medicines that are authorized or being studied in clinical trials in the European Economic Area (EEA).

The new system makes it easier for marketing authorization holders and sponsors of clinical trials to report suspected adverse reactions and allows for better analysis of this information for the benefit of patient safety in Europe.

According to the EMA, the enhancements and expected benefits of the new EudraVigilance are:

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