Interview: Impact of CTIS on TMF Management

The Clinical Trial Information System (CTIS) is a centralized, web-based platform developed by the European Medicines Agency (EMA) to streamline and harmonize clinical trial submissions and regulatory processes in the European Union (EU). The implementation of CTIS is expected to have a significant impact on the Trial Master File (TMF) in clinical research. It will lead to a more comprehensive, accessible, and transparent TMF. But what problems do TMF Manager face in while working with CTIS? Learn more about it in our interview!