As from the 31st of January 2022, the EU Regulation for research involving Medicinal Products (Clinical Trial Regulation, CTR) was ratified.

Under this regulation, sponsors submit the application for the medical-ethical assessment of their research involving medicinal products via an EU web portal, the Clinical Trial Information System (CTIS).

More information about the application for a CTIS account and other practical matters regarding CTIS can be found in this Research Roadmap and on the page of the Clinical Monitoring Center (CMC)