Welcome to Trilotalk Episode 24! In this episode, Douglas and Nidhi will take you through an overview of the recently introduced EU-CTR (Clinical Trial Regulation) – a hot topic in our industry these days! As medical writers, we need to be aware of not only what the EU-CTR is but also how it impacts the documents we often write. Join us to find out more about it! We will talk about what the EU-CTR is, the pros and cons of the new process, how a CTA in the EU is structured, and touch upon associated transparency and public disclosure requirements.
