FAQ EU PAS Register
European Medicines Agency's Privacy Statement - European Union electronic Register of Post-Authorisation Studies (EU PAS Regis
Register of Studies questionnaire for publication
2022 ATTENDEE - PAS Meeting
REGISTRY SNAPSHOT: The European Union Electronic Register of Post-Authorization Studies (EU PAS Register) - Trial Assure
EU PAS Register Guide
Visitor Badges with Visitor Pass Registry Book
EU PAS Register Guide
Drug safety in pregnancy: review of study approaches required by regulatory agencies | bioRxiv
EU PAS Register Guide
Are risk minimization measures for approved drugs in Europe effective? A systematic review
Type of EMA requested PAS registered in ENCePP by 18 th October 2016 by... | Download Table
The EU register of post-authorisation studies: why is it important to register studies and lessons learned?
EU PAS Register Guide
EU PAS Register Guide
European Medicines Agency's Privacy Statement - European Union electronic Register of Post-Authorisation Studies (EU PAS Regis
EU PASS/PAES Requirements for Disclosure
Post-authorisation safety studies (PASS) | European Medicines Agency
EU PASS/PAES Requirements for Disclosure
A review of studies evaluating the effectiveness of risk minimisation measures in Europe using the European Union electronic Register of Post‐Authorization Studies - Vora - 2018 - Pharmacoepidemiology and Drug Safety - Wiley Online Library
