Our Services
Site Feasibility and Selection
Our trial feasibility and site selection service focuses on identifying qualified sites and investigators which meet key metrics, ensuring they align with your protocol requirements. We prioritize efficient matching to meet your target timelines and enrollment goals.
Project Management
Our project management service ensures seamless execution through effective site and vendor contract and budget negotiations, along with meticulous oversight of timelines and milestones. We also specialize in developing study tools and implementing risk mitigation strategies to guarantee project success.
Clinical Monitoring
Our independent clinical research monitors conduct on-site and/or remote visits from qualification, initiation, interim through to close-out, adhering to ICH E6 (R3) GCP guidelines. We ensure patient eligibility, maintain data integrity, resolve queries, and identify protocol deviations to support the success of clinical trials.
Trial Master File Specialists
Our eTMF specialists have experience with a variety of document management platforms. They will collect, maintain essential source records in accordance with the TMF Standard Model. We specialize in classification, ensuring compliance with ALCOA+ and preparing your organization for inspection readiness.