Clinical Operation

Our services cover the new drug development stage and phase IV of trials after the drug is marketed. We can comprehensively assist clients in clinical trials and development for multinational, regional or domestic new drug development. And the experienced trial monitoring team is able to deal with emergencies, and to ensure that the quality and efficiency of the trials meet the needs of the clients.

• Project Management of Trials

• Clinical site Qualification/Selection

• Clinical Trial Agreement Negotiation

• Clinical Fees Management

• Clinical Personnel Training

• Investigational Product Logistics

• Investigator’s Meeting

• Clinical Site Initiation

• Revise Clinical Trials Master File

• GCP Auditing

• SAE/SUSAR Management

• Health Authorities’ Inspection Handling

• Clinical Site Close-out