Supporting Ethical & Compliant Clinical Research
CliniHunt Research Services supports sponsors, CROs and investigators across all phases of clinical research with strong site management, regulatory compliance and quality oversight.
Our expertise spans multiple clinical trial designs and therapeutic areas. We ensure ethical conduct, patient safety and high-quality data throughout the clinical trial lifecycle.
Types of Clinical Research Studies
We support diverse study designs across clinical development
Treatment Trials
Evaluation of new treatments, drugs or interventions to assess safety and effectiveness.
Prevention Trials
Studies focused on preventing diseases using vaccines, medicines or lifestyle strategies.
Diagnostic Trials
Assessment of diagnostic tools for accurate and early disease detection.
Screening Trials
Identification of effective screening methods for early-stage diseases.
Quality of Life Studies
Research focused on improving patient comfort, symptom management and overall well-being.
Observational Studies
Observation of health outcomes without assigning specific treatments.
Our Role in Clinical Trials
As a Site Management Organization (SMO), CliniHunt Research supports clinical trial sites through every stage of study execution with a strong focus on compliance and quality.
- Site feasibility and selection
- Ethics Committee submissions & approvals
- Patient recruitment and retention
- Investigator & site staff coordination
- Monitoring readiness & compliance oversight
- Study close-out support
ICH-GCP
Compliance Driven
Ethics
Patient Safety First
Quality
High-quality Data
Timelines
Efficient Execution