Delivering Confident Clinical Research Execution
CliniHunt Research partners with sponsors and CROs to deliver ethical, compliant and operationally excellent clinical trial site management across India.
Site Feasibility
Rapid & data-driven
Study Start-Up
EC & regulatory support
Patient Recruitment
Optimized enrollment
Compliance Oversight
Audit readiness
Trusted Site Management Partner
CliniHunt Research collaborates closely with investigators, hospitals, sponsors and CROs to ensure smooth clinical trial operations with strong regulatory compliance.
- End-to-end site lifecycle management
- Experienced clinical research professionals
- Strong investigator & hospital network
Our Capabilities
Comprehensive clinical trial site management and support services
Site Management
Feasibility, EC submissions, documentation and coordination.
Investigator Support
Trained research staff, archival and operational assistance.
Clinical Trial Support
Patient recruitment, monitoring and study close-out.
10+
Years Experience
150+
Clinical Sites
300+
Trials Supported
ICH-GCP
Compliance Driven