About

This web supplement accompanies "Adherence to legislation and recommendations to publicly post protocols and results of post‑authorisation studies registered with European Medicines Agency: cross sectional study".

This simple static website uses HMA-EMA RWD Studies Catalogue's metadata to generate sponsor- and study-level statistics about adherence to legislation and recommendations regarding the publication of protocols and results of post-authorisation studies (PAS) registered in the EU.

Additionally, this website will aggregate information on the PAS status, the Risk Management Plan (RMP) in which the PAS is included, and the countries in which the PAS is conducted at sponsor level.

All sources and further information are available on GitHub and in the paper.