EU CTIS
2025 marks the end of a three year period where clinical trials were transitioned to CTR through the EU Clinical Trials Information System (CTIS). Key changes include the launch of a clinical trial map in March 2025, supporting the Accelerating Clinical Trials in the EU (ACT EU) initiative. Clinical Data Disclosure Europe provides the analysis and insights required to navigate the transition and the subsequent impacts.
Practical Operational Strategies to Manage CTIS Requirements
Hear from Radek Grabowski, Head of Registries, Clinical Trial Transparency at AstraZeneca to get a sense of how Clinical Data Disclosure Europe supports you in navigating CTIS in a 5 minute preview from a previous session.