欧州医薬品庁が発行した電子証明書の信頼性を確認する方法
EMA Account Management
CTIS - M16 How to populate the overall inspection outcome and update and cancel an inspection record
Organisation Management Service (OMS) Trouble Shooting Sessions for CTIS users
Organisation Management Service (OMS)
CTIS - M15 How to view and download CTs in the authority workspace
News Update Amsterdam wins bid to host EU medicines agency post-Brexit 20/11/17
Integration of EudraGMDP and OMS Webinar for industry
How to fill in the “Procedural Information” section of the eAF on the PLM Portal
Network users training for Regulatory Procedure Management 1st roll-out on IRIS
EUROPEAN MEDICINES AGENCY I EMA I INTRODUCTION I HINDI
EMA Account Management training webinar
How to fill in the “Finalisation” section of the eAF on the PLM Portal
Training recording: how to submit an application for orphan medicinal product designation using IRIS
Implementation of the clinical trials regulation
i-SPOC Registration
The European Medicines Agency and patient involvement in the drug approval process
