Comprehensive Clinical Trial Support
End-to-end site management and clinical trial support services ensuring ethical conduct, regulatory compliance and operational excellence across all study phases.
CliniHunt Research Services provides comprehensive site management and clinical trial support solutions, partnering with sponsors, CROs and investigators to deliver reliable, compliant and efficient study execution.
Site Management
Complete site lifecycle management including feasibility, ethics submissions, documentation and coordination.
- EC / IRB submissions
- Site feasibility & selection
- Study start-up activities
- Project coordination
Investigator Support
Operational and staffing support for investigators and research sites to ensure smooth trial execution.
- Experienced clinical research staff
- Archival & documentation support
- Site coordination assistance
- Ongoing operational support
Clinical Trial Support
Comprehensive trial support services to enhance quality, compliance and timelines.
- Patient recruitment & retention
- Monitoring & oversight
- Trial close-out activities
- Quality review support
Regulatory Support
Regulatory documentation and compliance support aligned with applicable guidelines.
- Regulatory submissions
- Compliance readiness
- Audit preparation
- Regulatory coordination
Patient Recruitment
Strategic and ethical recruitment approaches to meet enrollment targets efficiently.
- Patient identification strategies
- Enrollment planning
- Retention programs
- Community outreach
Quality & Compliance
Ensuring robust quality systems and compliance throughout the clinical trial lifecycle.
- ICH-GCP compliance
- Quality oversight
- Audit support
- Process improvement