EudraVigilance: Electronic Reporting of ICSRs in the EEA
Venue: Medical Products Agency
Event Date/Time: Oct 09, 2006 | End Date/Time: Oct 11, 2006 |
Description
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.