Remington-Davis

Remington-Davis

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Private Company

Funding information not available

Overview

Remington-Davis is a well-established, private clinical research site organization (CRO/Site) with over 30 years of experience managing more than 600 clinical trials. Its core value proposition lies in accelerating trial timelines through fast patient recruitment from a large, diverse database, rapid contract and IRB turnaround, and flexible, personalized trial management. Operating as a service provider rather than a drug developer, it mitigates sponsor risk by offering proven enrollment capabilities and high retention rates in a dedicated facility.

VaccinesCardiovascular DiseaseNephrologyImmunologyDermatologyEndocrinologyGastroenterologyOncologyInfectious diseasePulmonologyInternal medicine

Technology Platform

Integrated clinical trial site operations platform featuring a proprietary patient database (>19,000 individuals), multi-channel recruitment system (advertising, hotline, recruiters), community engagement networks, and leading-edge clinical trial data management technology for secure and accurate data collection.

Opportunities

Growing demand for sites that can rapidly enroll diverse patient populations, driven by persistent industry-wide recruitment delays and new FDA Diversity Plan requirements.
Expansion of decentralized trial models creates a need for sites with robust remote data management capabilities.

Risk Factors

Operational reliance on a single geographic site and a finite local patient database.
Intense competition from large site networks and academic centers.
Revenue dependency on the cyclical R&D spending of pharmaceutical and biotech sponsors.

Competitive Landscape

Competes with other independent clinical research sites, large site networks operated by global CROs (e.g., ICON, PPD), and hospital-based academic research centers. Differentiation is based on enrollment speed, patient diversity rates, personalized service, and three decades of site management experience.