1  Confirm applicant’s requirements.
2  HM responsible for drafting contract, including case, fees, time, goal and so on.
3  Choose Clinical Trial Hospitals.
4  Draft “Researchers Manual”,assist PI in drafting and completing clinical protocol.
5  Clinical protocol submitted for Ethics Committee’s approval.
6  Applicant sign clinical contract and protocol with hospitals.
7  Submit clinical protocol, hospitals and PI members to sFDA on record.
8  HM responsible for organizing clinical kick-off meeting.
9  Applicant provided all drugs for clinical trials.
10 Monitor clinical trial’s implementation and record according to GCP.
11 Hospitals draft clinical reports, and raw data should be filed.
12 HM hand over clinical reports and statistical reports to applicant after each clinical phase finished.