Clinical Research Services
Delivering structured operational coordination, site support, and documentation rigor across phase I–IV clinical studies in India.
Verified Clinical Service Portfolio
All services listed below reflect verified operational areas provided by ResearchPath. We operate strictly in compliance with approved study protocols and applicable ethical guidelines. We do not provide unverified or unapproved speculative offerings.
Clinical Trial Operations Support
Operational support for trial planning, site initiation, progress tracking, and day-to-day study workflow management.
- Study startup timeline development and milestone tracking
- Site initiation visit logistics and documentation collation
- Daily operational liaison between study sponsors, sites, and vendors
Clinical Research Coordination
Site-level coordination support to assist investigator teams with study documentation, subject appointment workflows, and query resolution.
- Subject appointment scheduling and protocol visit timeline management
- Informed consent documentation support under investigator oversight
- Assistance with Case Report Form (CRF / eCRF) completion and query tracking
Patient Recruitment Support
Ethical, protocol-compliant strategies to assist study sites in identifying, informing, and engaging prospective study participants.
- Development of ethics-approved patient awareness and information materials
- Design of structured pre-screening questionnaires based on eligibility criteria
- Site-level outreach workflow optimization for referring clinicians
Clinical Data Management Support
Assisting research teams with data entry verification, electronic CRF tracking, validation checks, and query reconciliation.
- Electronic Case Report Form (eCRF) completion tracking and backlog clearing
- Manual and programmatic data discrepancy generation and resolution tracking
- Source Data Verification (SDV) preparation support for clinical monitors
Site Feasibility & Selection Support
Objective evaluation of clinical trial investigator sites, assessing patient population, infrastructure, and investigative capacity.
- 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)
Regulatory Documentation Support
Support in preparing, organizing, and reviewing clinical study documentation for Ethics Committees and regulatory submissions.
- Compilation of Institutional Ethics Committee (IEC) submission dossiers
- Informed Consent Form (ICF) formatting and local language translation coordination
- Subject Information Sheet (SIS) readability review and standardization
Need Guidance on Your Specific Clinical Trial Parameters?
Speak directly with our clinical operations coordinators in Pune to review your protocol requirements, site needs, and documentation timelines.