EudraVigilance registration: questions and answers

This page answers questions users may have related to the registration process for the EudraVigilance reporting system for adverse drug reactions as described in EudraVigilance: how to register.

They are available as PDF document, too:

1. Who should register with EudraVigilance

2. EudraVigilance registration process

3. Introduction of a 'regulatory contact point' for marketing authorisation holders (updated 27/03/2017)

4. Delegation of reporting tasks

5. Merge of organisations

6. Separation of organisations

7. Updating an organisation category (new topic)

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