Clinical Data Publication (Policy 0070) re-launch - EMA webinar
Clinical Trials in the EU - short version
CTIS – M08 How to assess an initial clinical trial application in CTIS – Part I
Authoring Efficiencies and Cross-functional Strategies: Clinical Study Report and Beyond
EMA workshop on patient experience data in medicines development and regulatory decision-making
How to Best Prepare for an EMA Policy 0070 Submission
Webinar on transparency rules for the EU Clinical Trials Information System CTIS
Webinar — Comparing CTA Submission (EMA/Health Canada) to IND Applications (FDA) for Phase I Trials
CTIS – M08 How to assess an initial clinical trial application in CTIS – Part II
Clinical Trials Information System (CTIS) bitesize talk: Notifications - Part 1
Writing the Clinical Study Report
Reactivation of EMA Policy 0070 Introduction and key recommendations for a successful Publication 20
[Efficacy] E3
Webinar for SMEs and Academia on CTR/CTIS
EMA webinar on Article 117 of the Medical Devices Regulation EU 2017/745
G5 Input CTD application, Output regulators’ assessment report
Clinical Trials Information System CTIS Walk in Clinic
Meeting the EU Regulation: Plain Language Summaries & Protocol Synopses
CTIS Walk in Clinic
Clinical Trials Information System (CTIS): Walk-in clinic