SCOPE offers full clinical data management services for Phase I-IV clinical trials and non-interventional/post-authorization studies. We draw on experience in various therapeutic areas gained through complex long-term projects, allowing us to create reliable timelines and ensure timely delivery of data. Our focus on quality and integrity of data and our attention to detail while maintaining a global perspective ensures comprehensive planning and adequate control for any project.
Our committed team has worked together for over 20 years. Clinical data management, clinical operations and our statistics teams work hand in hand to identify, mitigate and monitor risks throughout the project.
Our ability to construct studies on several EDC platforms allows us to offer the best fitting tools tailored to your specific project while maintaining full oversight throughout the study. To find out how we can support all your clinical data management needs, simply contact us.