Terms And Conditions

Terms & Conditions
ENCePP Database of Research Resources


The European Medicines Agency (EMA) has developed the ‘ENCePP Database of Research Resources’ to catalogue the research centres and networks participating in ENCePP. This electronic registry is aimed at collecting and presenting information about research expertise & capacity and providers of potential data sources available for the conduct of pharmacovigilance and pharmacoepidemiology studies.


When you register a centre, network or data source, or update existing entries, you confirm that the information entered is true, accurate and current. Registration is also an acknowledgement that the information entered will be made available to the public via the ENCePP website. All provisions of the EMA website Privacy Policy apply.

It is the responsibility of each individual research centre and network to enter and to keep its own information up-to-date. Participating centres and networks may edit their information at any time. By registering in the Database of Research Resources, you commit to review and update your entry(ies) regularly, and, as a minimum, at least every twelve (12) months. For that purpose, a periodic reminder to do this will be sent.

An acknowledgement will be dispatched within two weeks of submission. The ENCePP Secretariat reserves the right to reject any submission for registration deemed incomplete or inadequate or where the centre, network or data source is not thought to comply with the requirements in place at that time.

I accept the Terms and Conditions