Site Services

Syncorp Health understands the site Management is a critical part of any trial success. As per the site Management team performs these key tasks (but not limited to these listed).

  • Site identification and activation
  • IRB SOP writing and assist in CDSCO registration
  • IRB Dossier preparation for proposed clinical trial study as per IRB SOPs
  • IRB submission and follow up till approval
  • Site audit, for internal quality review purpose
  • Protocol and study specific training for the site team
  • GCP training for IRB members and site personnel (PI, COI, CRC etc.)

We offer a comprehensive portfolio of services which can be tailored to meet the customer needs
Clinical Operations Therapeutic Area of Experience Site Feasibility
Site Selection Study Startup Patient Recruitment
Site Services Project Management Site Monitoring
Data Management Biostatistics & Programming Medical Writing
Regulatory Services Safety Services Quality
Consulting Services Vendor Management Technology
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