The EU regulation 536/2014 (Clinical Trial Regulation, CTR) became effective on January 31, 2022. All new applications for clinical trials with medicinal products can now be submitted electronically via the Clinical Trials Information System (CTIS). As of January 31, 2023, any new application must be submitted via the new portal.

For the application in the CTIS portal, all institutions involved in a clinical trial are assigned to specific organization IDs (ORG IDs) and location IDs (LOC IDs; corresponding to the postal address). At MHH, the ZKS has been entrusted by the executive board with the implementation of the CTR. Please contact the ZKS to obtain the organizational and locational ID data for MHH submission: regulatory.zks@mh-hannover.de.