EudraVigilance: Electronic Reporting of ICSRs in the EEA

Venue: Medical Products Agency Box 26

Location: Uppsala, Sweden

Event Date/Time: Oct 23, 2006 End Date/Time: Oct 25, 2006
Report as Spam


This course will be the only training programme officially recognised by the EMEA. The EMEA will present successful candidates with a 'Certificate of Completion' based on a competency assessment at the end of the course.

The EudraVigilance training programme is open to Contract Research Organisations (CROs), Consultants and other organisations with an interest in the EudraVigilance project. However, it should be noted that the persons attending the training will only be given access the EudraVigilance training environment for a period of two months.

After this period the EudraVigilance system will only be available for these organisations if they act on behalf of a Marketing Authorisation Holder (MAH) or a Sponsor of a Clinical Trial and that this is notified to the EMEA in writing and through the EudraVigilance registration process.