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About EudraVigilance |
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The European Medicines Agency with the Drug Information Association (DIA) as conference organizer, have initiated a large-scale EudraVigilance user training program.
The EudraVigilance training program aims to provide participants with the skills and competencies required to efficiently manage the new concepts of electronic reporting in the European Economic Area (EEA).
Regular training sessions will take place at the European Medicines Agency. Upon successful completion of a three-day training course, participants will receive a 'Certificate of Completion'. The course is open to regulators and pharmaceutical companies in the enlarged European Union. It will also be open to academic sponsors following the implementation of the 'Clinical Trial' Directive 2001/20/EC.
Related Courses
Reference Documents
Competency Assessment
Eudravigilance FAQs
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