Provide writing and professional review services for clinical trial related documents, including trial protocols, case report forms, informed consent forms, study medical records, investigator manuals, clinical research reports, etc.
● Feasibility Study of the Project
● Preparation before the launch of the center (screening of research centers, organization of researcher conferences, ethics declaration, application for personnel and heritage management, negotiation and signing of research center contracts, etc.)
● Research center launch and training
● Clinical trial monitoring
● Quality control of clinical trials
● The research center is closed
Based on a comprehensive project management standard operating procedure (SOP), clinical trial management system (CTMS), tools, and training system, and adhering to a customer-centric service philosophy, the GCP ClinPlus project manager, as the project leader, will provide you with a one-stop solution for overall clinical trial management, including developing project scope, schedule, quality, funding, risk, team, communication, and other related management plans, tracking and reporting project progress, identifying project risks, resolving project issues, and ensuring that deliverables meet expectations.
Our project management services
● Provide customers with overall project management strategies and solutions based on project characteristics and customer demands
● Develop an overall project management plan that includes project team, schedule, quality, cost, risk, communication management, etc
● Develop feasible project onboarding plans and strategies
● Develop a project schedule and continuously monitor progress risks and resolve schedule issues throughout the project progress process
● Refine and develop a project quality management plan to ensure that project quality meets GCP and relevant regulatory requirements
● Refine and develop a project risk management plan that includes risk identification, prevention, and response strategies, conduct continuous risk monitoring, and update the risk register
● Develop a detailed project communication plan based on the contract, project characteristics, and customer needs
● Develop a project cost management plan and track the use of expenses
● Review SAE reports, archive signed scanned copies of SAE reports and fax receipts, regularly summarize and report to the sponsor (based on specific project requirements), and assist other departments in handling SAE related issues.
● Comprehensive and integrated pharmacovigilance services throughout the entire product lifecycle:
● Review the Chinese and English versions of SAE
● Archive signed SAE report and fax receipt
● Regularly summarize and report
● Assist in handling SAE related issues
Data Management and Statistical Analysis
● Data management: Provide data management services for EDC projects and paper projects in various treatment fields
● Biostatistics: Providing comprehensive biostatistics services for clinical trial design, analysis, and reporting
● Statistical programming: Provide comprehensive statistical programming related services, especially for the implementation and electronic submission of CDISC
Research Center Inspection
● According to project requirements, conduct inspections on 50% to 100% of research centers during different project lifecycles
● National Bureau of Verification, Cooperation and Response
● Root cause analysis of the problem
● CAPA development/training/tracking