Overview
Since 31 January 2023, it has been mandatory for sponsors to submit all initial clinical trial applications via CTIS. In less than 7 months, from 31 January 2025 onwards, sponsors will need to comply with their obligations under the CTR and its Delegated Acts for all clinical trials conducted in the EU/EEA.
The virtual event aims to support sponsors of clinical trials in proceeding with the transition to meet the deadline of 31 January 2025. Speakers will share detailed metrics on transitioned clinical trials. In addition, comprehensive guidance and practical examples regarding the subsequent steps in transitioning trials will be presented.
Furthermore, the revised transparency rules for the Clinical Trials Information System (CTIS) will become applicable on 18 June 2024, with the launch of a new version of the CTIS public portal. During the event representatives from EMA will provide an overview of the revised transparency rules as well as a demonstration of the new functionalities of CTIS new public portal
Ample time is foreseen for Q&A. The faculty invites participants to submit related questions by 08 October latest. Submit your questions to emaevents@diaglobal.org.
Program Committee
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Ana Zanoletty Perez Head of Clinical Trials Transformation Workstream
European Medicines Agency, Netherlands -
Francesca Scotti CTIS Transparency Lead
European Medicines Agency, Netherlands -
Marianne Lunzer, DrMed Assessor, Dept of Clinical Trials, Federal Office for Safety in Health Care
AGES, Austria -
Peter Richard Arlett, MD, FFPM, FRCP Head Data Analytics and Methods Task Force
European Medicines Agency, Netherlands -
Scott Feiner Senior Manager, Trial Disclosure
AbbVie, United States
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