Clinical Research Management Office
The Clinical Research Management Office (CRMO) is a joint office of New Territories East Cluster (NTEC) and CUHK dedicated to enhancing the quality standards, efficiency and compliance of clinical trials. CRMO implements clinical research policies set by its Clinical Research Management Committee and coordinates activities to improve the safety of research subjects, the integrity of research conduct and the compliance of regulatory requirements in accordance to Good Clinical Practice (GCP). CRMO also coordinates with various stakeholders involved in clinical research, including the Department of Health, National Medical Products Administration (NMPA), study sponsors (pharmaceutical and biotechnology companies), contract research organisations, as well as investigators and research units.
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