🏥 Trinetra Clinical Research Services

Our Services

Trinetra provides complete clinical trial management and site support services for Sponsors, CROs, Hospitals and Investigators.

🏥

Site Management Services

  • Site identification and feasibility assessments
  • Investigator identification and engagement
  • Study start-up and activation support
  • Site coordination and communication
  • Clinical trial documentation management
  • SOP implementation and compliance monitoring
👥

Patient Recruitment & Retention

  • Access to large patient databases
  • Recruitment planning and execution
  • Patient counselling and retention strategies
  • Community and physician outreach support
📋

Regulatory & Ethics Support

  • DCGI and regulatory documentation support
  • Ethics Committee submissions and coordination
  • Regulatory compliance management
  • Audit and inspection preparedness

Clinical Operations Support

  • Clinical Research Coordinator (CRC) support
  • Data entry and source documentation support
  • Monitoring visit coordination
  • Investigator meeting coordination
  • Study tracking and reporting

Quality Assurance

  • Internal quality checks and compliance reviews
  • GCP compliance monitoring
  • Documentation quality review
  • Inspection readiness support
📊

Reporting & Communication

  • Real-time project reporting
  • Continuous Sponsor & CRO communication
  • Study tracking dashboards
  • Issue escalation & resolution
Clinical trial documentation
End-to-End Delivery

From Feasibility to Close-Out

Our standardized processes and trained clinical research staff enable smooth study conduct from the earliest feasibility phase to final archival, with a relentless focus on quality and compliance.

Discuss Your Study

Need a reliable SMO for your next clinical trial?

Trinetra offers proven site management, recruitment and regulatory expertise across India.

Partner With Us