ENCePP Resources Database
The Resource Database is an electronic index of available EU research organisations, networks and data sources, including patient registries, in the fields of pharmacoepidemiology and pharmacovigilance, and is a key component of the ENCePP web portal. All information contained in this database is provided and maintained by the listed organisations, data providers or registry holders.
The Resource Database includes information on expertise and research experience across Europe and serves as a hub for both researchers and study sponsors seeking to identify organisations and data sets for conducting specific pharmacoepidemiology and pharmacovigilance studies in Europe.
If you and/or your organisation are interested and/or actively involved in performing research in the field of pharmacoepidemiology and pharmacovigilance and would like to join the ENCePP network please click “Add Centre/Network” or contact us at
Existing patient registries are invited to enter their details in the Inventory of Data Sources. Guidance on how to upload patient registries is provided in the document “ENCePP Resource Database – Inventory of Patient Registries”.
Click “Add Data Source” if you are managing a data set or patient registry that can be used in pharmacoepidemiology and pharmacovigilance research.
Click “Edit Resource” if you already have an entry in the Resources Database and would like to update it.
If you wish to resume a draft application saved previously (but not submitted yet) or update a returned application, please follow the link:
Resume Draft/Returned application.
(By adding a centre or network/collaboration, you automatically join the ENCePP network)
For the UK, as from 1.1.2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI
