A Complion Feature Article
Varied study requirements, increasing protocol complexity, multiple amendments. Sponsors simply want to ensure the data produced by a study is sound.
Research sites often feel they need to comply with what sponsors require. While sponsors may have preferred tools and technologies for handling study data, they often are open to sites using their own systems they have a proven history.
Access the article and learn:
- What are clinical research sites’ perspectives on the most time-consuming administrative tasks related to regulatory compliance.
- Gain insight into what has caused the burden associated with administrative tasks for a single study to increase over the past two years.
Access the article today!