This is a first of a series of Webinars EUCROF is offering to facilitate the understanding and future operational work with the new EU Clinical Trial Regulation (CTR) and the Clinical Trial Information System (CTS) 

With the EU CTR becoming effective on 31 January 2022, a new era of clinical trials with medicinal products has begun in the EU/EEA. In this Webinar, the transitional provisions will be explained and different scenarios will be discussed around this topic. Finally, the CTR is offering new concepts in comparison to the EU Clinical Trials Directive (co-sponsorship, low-intervention clinical trials) – those topics will also be discussed in this Webinar. Don’t miss this opportunity! 

The Webinar will take place on 30 March from 10:00 am to 11:30 (CET).  

The registration deadline is 29 March 2022 and it is directed to Sponsors, Principal Investigators, Co-Investigators, Study Coordinators, Project Managers, Administrative Managers, Providers, and any other qualified person involved in Clinical Trials. 

More information and registration here: 

https://www.eventbrite.com/e/eu-clinical-trial-regulation-5362014-ctr-registration-288183433407  

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By Published On: March 15th, 2022Categories: News0 Comments