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