Award-winning experts share their detailed and actionable insights to inform
the future of pharma and biotech.
CURRENT WEBINAR
EU CTR Compliance and Success: Navigating Updates and Preparing Submissions for the EU CTIS Portal
As of January 31, 2023, Sponsors are required to submit all new trial applications for authorization in the European Union through the Clinical Trial Information System (CTIS) in compliance with the new European Union Clinical Trials Regulation (EU CTR).
In this webinar, a cross-functional team, including clinical trial transparency specialists and medical writers, will share best practices and insights to help Sponsors better prepare their submissions for the EU CTIS portal.
.png?width=130&name=MMS%20logo_without%20Tagline%20(Full%20Color).png "MMS logo_without Tagline (Full Color)")
.png?width=160&height=104&name=MMS_logo_wTagline-(white).png "MMS_logo_wTagline-(white)"){kind=logo}
.png?width=1200&height=628&name=MicrosoftTeams-image%20(27).png "EU CTR Compliance and Success: Navigating Updates and Preparing Submissions for the EU CTIS Portal")
.png "Strategies for Navigating ICH E9(R1)")
