Service

01

Study support Service
We provide services to ensure efficient study conduct at hospitals conducting clinical research and clinical trials.

minus plus

  • Support for subject enrollment (recruitment advertising and call center operation)
  • Training and management of site staff
  • Preparation for site inspections and regulatory audits, with follow-up
  • Administrative tasks related to study management and regulatory authorities

02

CRC Out-sourcing Service
We offer professional CRC (Clinical Research Coordinator) services tailored to the specific needs of each study.

minus plus

  • Study schedule management
  • Subject enrollment and registration
  • Sample collection, handling, and storage
  • Preparation and management of source documents
  • Case Report Form (CRF) data entry and management
  • AE/SAE reporting and management
  • Preparation and maintenance of essential study documents
  • Participation in site initiation, monitoring visits, audits, and inspections
  • Comprehensive CRC support for all study-related activities

03

IRB Reporting Service
We provide timely and accurate reporting services to the IRB, ensuring compliance and reliability throughout the study.

minus plus

  • Submission for initial review, amendment review, and continuing review
  • Interim, final, and result reports
  • SAE and SUSAR reporting
  • Protocol deviation/violation reporting