Choosing the Right Partners. Building Research-Ready Environments
At InSight Health Clinical, successful trials start with capable sites and compliant laboratories. Our Laboratory and Site Evaluation services ensure clinical research begins with the right infrastructure, personnel, and regulatory readiness.
From feasibility assessments to on-site audits, we evaluate every aspect of trial readiness, so sponsors can make informed decisions, mitigate delays, and safeguard study integrity from day one.
What We Offer
Pre-Study Feasibility & Site Selection
We assess site qualifications based on patient populations, past performance, staffing, infrastructure, and local regulatory environment.
Laboratory Capacity Assessment
We evaluate labs for certification status, equipment validation, turnaround time, QA/QC protocols, and GCLP adherence.
Site Readiness Audits
We conduct structured audits that review SOPs, PI availability, staff training, ethics approvals, and compliance with GCP standards.
Corrective Action Planning
If gaps are identified, we support sites and labs in developing realistic action plans and timelines for remediation, ensuring readiness for activation.
Site Support & Follow-Up
Post-evaluation, we provide mentorship and oversight to help sites and labs maintain standards throughout the trial.