Key Transition Timelines For Clinical Trials Regulation (CTR)

With the clock ticking down, navigating the labyrinth of timelines and requirements for transitioning ongoing clinical trials in the EU to the Clinical Trials Regulation (CTR) framework becomes paramount. This infographic delves into the critical milestones, from establishing harmonization strategies to submission deadlines, and highlights the time frames crucial for compliance. With up to 106 days for application review and additional requirements extending the process, staying ahead is paramount.

Explore our infographic to map out the path to CTR compliance and ensure a seamless transition for ongoing clinical trials.