Publications

The European post-authorisation study (EU PAS) register is a repository launched in 2010 by the European Medicines Agency (EMA). All EMA-requested PAS, commonly observational studies, must be recorded in this register.

The ENCePP Code of Conduct provides a framework for scientifically independent and transparent pharmacoepidemiological research. Despite becoming a landmark reference, practical implementation of key provisions was still limited.

Teaser?

Systematic overview of data sources for drug safety in pregnancy research

The European Network of Centres for Pharmacoepidemiology and Pharmacovigilance survey of methodologies for European Union publicly funded multi-database safety studies

ENCePP considerations of non interventional studies