太阳成集团tyc539(中国)百度百科

1. Essential Documents Preparation (Protocol, CRF, ICF and etc)

2. Study Start-up Investigator and Site Selection, Investigator Meeting Management, IEC/IRB Submission, Site Clinical Study Agreement

3. Monitoring

4. Project Management

5.QA & QC

6. Medical Affairs and Pharmacovigilance

7. Clinical Study Report (CSR) Writing