Site Feasibility & Selection Support
Objective evaluation of clinical trial investigator sites, assessing patient population, infrastructure, and investigative capacity.
What This Service Involves
Selecting the right investigative sites is fundamental to trial safety, recruitment velocity, and protocol compliance. ResearchPath conducts thorough site feasibility evaluations across India, assessing patient demographics, departmental infrastructure, equipment calibration, and investigator bandwidth.
Who It Is Intended For
Scope of Support
Our team provides disciplined coordination across the following agreed operational parameters:
- Customized site feasibility questionnaire design tailored to protocol parameters
- Site identification across diverse therapeutic areas and geographic clusters in India
- Infrastructure verification (pharmacy storage, -80°C freezers, emergency facilities)
- Investigator bandwidth assessment and competitive trial workload analysis
- Historical recruitment rate evaluation in relevant therapeutic areas
- Consolidated site feasibility scoring and recommendation reports
Operational Workflow Stages
Criteria Definition
Define must-have vs nice-to-have site requirements based on protocol complexities.
Site Outreach & Screening
Distribute structured questionnaires to shortlisted investigators and clinical departments.
Verification & Qualification
Evaluate site facilities, Ethics Committee meeting frequencies, and staff qualifications.
Feasibility Dossier
Deliver a comparative site ranking report highlighting operational strengths and potential risks.
Expected Deliverables
- Impartial, evidence-based evaluations free from institutional bias
- Verification of documented investigator qualifications and current trial commitments
- Validation of claimed patient pool numbers through hospital registry sampling
- Confidentiality agreements executed prior to exchanging proprietary protocol synopses
Note: ResearchPath provides coordination and operational support. We do not provide guarantees regarding regulatory approval decisions, trial clinical efficacy, or patient recruitment targets.
Frequently Asked Questions
How long does a typical site feasibility assessment take?
A standard feasibility evaluation covering 5-15 potential sites in India typically takes between 2 to 4 weeks depending on protocol complexity and investigator responsiveness.
Do you conduct on-site qualification visits?
We support both desk-based initial assessments and physical site inspection coordination depending on sponsor project requirements.
Discuss Your Clinical Requirements
Provide your study parameters or operational needs below. Our clinical operations team will review your specifications and contact you directly.
Important Notice: This portal is dedicated strictly to organizational, sponsor, and investigator inquiries. Please do not submit patient-identifying health information (PHI) or personal medical records through this form.
Operational Office
406, B Wing, City Vista, Kharadi, Pune, Maharashtra, India.
Phone: +91 91464 52014
Email: info@researchpath.in