ECRIN Campus for regulatory and ethical requirements
The ECRIN database for regulatory and ethical requirements to be met in clinical trials across Europe is now available to the public.
ECRIN provides a central resource for information about clinical trial regulatory and ethical requirements, covering over 22 European countries and multiple study types such as clinical drug trials, clinical investigations of medical devices, combination drug-device studies and nutritional studies.
ECRIN Campus can be used to locate country-specific competent authorities and ethics committees, to consult a summary of requirements for each country, and to browse related documents, such as applicable regulations and guidelines. It can be easily searched by country, study type, or a combination of both, to find relevant information.
Access the ECRIN Campus here