Investigators Training
CCRB has been working with the Hospital Authority to offer a series of training programs for Clinical Investigators and other clinical research professionals. The programs were designed to give clinical researchers an overview on the conduct of clinical research based on ICH GCP guideline. The program contents familiarized the participants with the GCP guidelines and showed the participants how to implement these regulation and guidelines to produce quality clinical researches.
Clinical Investigator’s Training (One-day Program)
- HA’s Policy and Infrastructure on Research Ethics
- The Responsibilities of Investigator
- Design of Clinical Trials and Other Source Documents
- Clinical Study Agreement
- Enrollment of Trial Subjects
- Clinical Trial Monitoring
- Inspection and Audit
- Clinical Trial Closeout