How CTIS is changing the landscape of clinical trials?
The Clinical Trials Information System (CTIS) is a centralized database that supports the conduct of clinical trials in the European Union (EU). It was launched in January 2022 and is a key component of the Clinical Trials Regulation (CTR), which aims to improve the efficiency and transparency of clinical trials in the EU. The CTIS has a number of features that make it a valuable tool for clinical trial sponsors, researchers, and Regulatory authorities.
These features include: