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Clinical Operations

Clinical Operations is our “bread and butter,” our core service solution. We take pride in our standardized project clinical management system and processes, low turnover rates, expert experienced and professional project management and audit teams, and extensive local networks of resources (more than 20 major cities) in operational efficiency and reduction in R&D costs cost-effective coverage – with staff located in all in the key clinical trial locations around when you are running study in Mainland China.

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    • Clinical Operations

      It’s our vision to ensure that your product has the best opportunity to reach patients in need. 

    Project Management & Clinical Operations

    It’s our vision to ensure that your product has the best opportunity to reach patients in need. We believe in the potential of your innovations, treating your clinical research project as if it was our own and personalizing our solutions to suit your exact needs, helping you safely advance your drug development at speed.

    Clinical Operations is our “bread and butter”, the CSC core service solution. We take pride in our standardized project clinical management system and processes, low turnover rates, expert experienced and professional project management and audit teams, and extensive local networks of resources (more than 20 major cities) in operational efficiency and reduction in R&D costs cost-effective coverage – with staff located in all in the key clinical trial locations around when you are running study in Mainland China.

    Our network of investigators, study personnel and high-performing sites are ready to support your study at following parts.
    • Sharing knowledge and bring extensive experience to clinical development plan of your product.

    • Improving and accelerating recruitment and retention. Our team works closely with our clinical investigator to understand and document patient pathways, create study site profiles and validate protocols that reduce patient and caregiver burdens.

    We can provide you with the following services:

    • Feasibility Assessments

      Study Feasibility ~Assessment

      Site/Investigator ~Identification

      Site Feasibility Assessment & Qualification

    • Clinical Strategy & Planning

      Study Planning & Execution 

      Risk Identification & Management

    • Project Management

      Project Oversight and Management

      Project Team Coordination and Communication

      Study Training

      GCP Training

      Periodic Status Reports

      Third Party Management

      Quality Control

      Trial Master File Management

    • Clinical Monitoring – Site Initiation to Site Close-out

      EC/IRB Submissions

      HGRAC Submissions

      Site Initiation

      Investigator Meeting Planning and Execution

      IP Management

      Clinical Supplies and Logistics Management

      Investigator Site File Management

      SAE Management

      Issue and Query Resolution

      Site Close-out