EastHORN will present the new CTIS at RAPS Chapters
We are happy to invite everyone to join our webinar on the new Regulatory submission pathway in the European Union.
Join our Zoom session on June the 1st at 8:00 PT, and you will have the opportunity to find out more about the new CTIS, and address your questions and concerns to our Regulatory specialists, Emilia Redaszek, and Blanca San Millan, Senior Regulatory Leads at EastHORN – A Novotech Company.
During this engaging 40 minute session, followed by a Q&A session, you will gain valuable insights into the latest changes in the EU clinical trials submission process and their impact on the clinical trial regulatory strategy. Blanca and Emilia will share practical aspects and their own experience, providing you with a comprehensive overview.
Topics to be discussed:
- Top-level summary of the new clinical trial submission process in the EU countries
- Understanding how the new submission process works and its impact on document preparation, submission strategy, and timelines
- Learning practical aspects and gaining insights from real life clinical trial submissions via CTIS
- Overview of ongoing study transitions to CTIS
Don’t miss out on this opportunity to stay up-to-date with the ever evolving landscape of clinical trials in the European Union.
Register here to secure your spot and mark your calendar for June 1st at 8:00 PT.