CUHK CTC supports study teams in preparation of clinical research, including clinical trial agreement vetting, application for hospital approval/clinical trial insurance and tracking on ethics application status. To obtain all the required regulatory approval documents, typically it takes 4-5 months.

CUHK CTC supports the initiation and the conduct of clinical research, including general consultation, site monitoring to ensure the study is conducted smoothly and in compliance with applicable guidelines and regulations.

CUHK CTC supports study closure activities to complete the last step of clinical research, including study document archiving and investigational products disposal.