Webinar: Best Practices for EU CTR Compliance Using Vault

From 31 January 2023 onwards, all clinical trial applications will have to be submitted via CTIS, in accordance with EU Clinical Trial Regulation 536/2014. This webinar focuses on the regulation’s impact on your business processes and how Veeva Vault applications support the new regulatory requirements.

Visit our hub for best practices, tips and tricks, and all the latest news about the EMA Clinical Trial Regulation.

Interested in learning more about how Veeva can help?