Post-authorization studies (PAS): European & American approach
EU PAS Register Guide
European Medicines Agency's Privacy Statement - European Union electronic Register of Post-Authorisation Studies (EU PAS Regis
EU PAS Register Guide
FAQ EU PAS Register
FAQ EU PAS Register
EU PAS Register Guide
Post-authorisation safety studies and the EU PAS Register, ENCePP ...
EU PAS Register Guide
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
2023 ATTENDEE - PAS Meeting
EU PASS/PAES Requirements for Disclosure
Are risk minimization measures for approved drugs in Europe effective? A systematic review
Register of Studies questionnaire for publication
European Medicines Agency's Privacy Statement - European Union electronic Register of Post-Authorisation Studies (EU PAS Regis
Visitor Badges with Visitor Pass Registry Book
Drug safety in pregnancy: review of study approaches required by regulatory agencies | bioRxiv
Post-authorisation safety studies (PASS) | European Medicines Agency
PDF) Overview of the EU PAS register post‐authorization studies performed in Europe from September 2010 to December 2018
EU PAS Register Guide
Overview of the EU PAS register post-authorization studies performed in Europe from September 2010 to December 2018
EU PASS/PAES Requirements for Disclosure
EU PAS Register Guide
Type of EMA requested PAS registered in ENCePP by 18 th October 2016 by... | Download Table
EU PAS Register Guide
