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FAQs

Below are frequently asked questions about DIA’s EudraVigilance training offerings. Click here for more questions and answers about pharmacovigilance and EudraVigilance, available at the EMEA website.



What is EudraVigilance? How do I register with EudraVigilance at the EMEA? What is the role of the DIA in the training? Why should I register for this training course? For whom has the EudraVigilance Training Programme been designed for? Who can register for this training course? What is included in the registration fee? How do I get to the EMEA? When does the course start and end? What happens if I do not pass the Competency Assessment? How do I register for a training course?


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FAQs

What is EudraVigilance?

EudraVigilance is the European data-processing network and management system, established at the European Medicines Agency (EMEA) to support the electronic exchange, management, and scientific evaluation of Individual Case Safety Reports (ICSRs) related to all medicinal products authorised in the European Economic Area (EEA). EudraVigilance also incorporates data analysis facilities and is therefore regarded as one of the main pillars of the European Risk Management Strategy, which aims to strengthen the conduct of pharmacovigilance in Europe.

Further information is available on the EMEA website.

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