General

The European Medicines Agency has developed the ‘ENCePP Database of Research Resources’ to catalogue the existing European research centres participating in ENCePP and the available European data sources. This electronic registry is aimed at collecting and presenting information about the centres’ expertise and capacity and the data available for conducting pharmacovigilance and pharmacoepidemiology studies in response to a particular research question.

Membership and Registration

When you register your centre, or a data source, or provide subsequent updates to existing database entries, you confirm that this information is true, accurate, current and complete. You agree that ENCePP may use the information you provide to us according to the Privacy Policy on our Website.

If you register with ENCePP, you agree to accept responsibility for all activities that occur under your account or password.

It is the responsibility of each individual research centre and data source provider to enter its own information and to keep this information up-to-date at all times. By submitting an application to be included in the database of Research Resources, you commit to review and update your database entry(ies) regularly, but at least every twelve (12) months. For that purpose, periodic reminders will be sent out. Entries that have not been reviewed within one month of receipt of a reminder will be removed from the registry. Centres may edit their information at any time.

By submitting their data, research centres and data source owners acknowledge that all information is accessible to the public at the ENCePP website.

The ENCePP Secretariat reserves the right to reject any submission for registration deemed incomplete or inadequate. An acknowledgement will be dispatched within two weeks of submission.