Registration of clinical trial sites in CTIS (Clinical Trials Information System)

Clinical trial sites where clinical trials of medicinal products will be conducted must be registered in the OMS (Organisation Management Service) of the EMA (European Medicines Agency).

Basic information on what an OMS is can be found on the EMA website.

Registration instruction are available in the OMS Web User Manual:

 pdf.pngOMS Web User Manual.pdf, soubor typu pdf, (8,13 MB)

December 14, 2021

Department of Clinical Trials on Pharmaceuticals