Since 2003, Beijing Haimiao Pharmaceutical Technology Co., Ltd(HM) has finished  numbers of IVD ‘s clinical trials,including new IVD’s clinical research.Accumulated rich experience and extensive clinical relationship, have the ability to provide a full range of clinical research services.
Flow Chart for Clinical Trial

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 clinical protocol with clinical hospitals based on all clinical related materials.
5 Clinical protocol submitted for Ethics Committee’s approval.
6 Applicant sign clinical contract and protocol with hospitals.
7 Applicant provided all IVD regents and related machines.
8 HM monitor clinical trial’s implementation and record.
9 Hospitals draft clinical reports, and raw data should be filed.
10 HM hand over all data (clinical contract, protocol and reports) to applicant after signed and sealed by hospitals and HM.