Clinical Research Management Office (CRMO)

Clinical Research Management Office (CRMO) is a set-up joint office of NTEC and CUHK to enhance the quality standard, efficiency and compliance of clinical trials.  CRMO implements clinical research policies set by CRMC (Clinical Research Management Committee) and coordinate 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 coordinate and liaise with various stakeholders in clinical research, including Department of Health, China-FDA, study sponsors (pharmaceutical company/biotechnology company) and contract research organization (CRO), as well as investigators and research units. 

Tel: 3505 4276