Central Laboratories Products/Services

  1. Medrio EDC Software 5/15/2024

    More than just an electronic data collection tool, our robust clinical data management system combines an intuitive user interface, seamless online and offline data capture capabilities, and comprehensive data management for clinical trials in a single solution.

  2. TrialKit Coder for Medical Coding 12/29/2025

    Code and approve clinical trial data from any device and keep your safety and efficacy data clean, consistent, and ready for analysis.

  3. Collect RWE With Natural History Studies 9/20/2023

    Developing a therapy for a rare or ultra-rare disease is life-changing work with unique challenges. Examine how natural history data is being used to inform the clinical development process.

  4. Commercial Alerts: Now Available With EHR, Claims And Prescription Data 3/27/2025

    Identify & engage healthcare professionals (HCP) treating eligible patients—in near real-time

    Timely physician engagement is critical to therapy adoption. Quest Diagnostics combines near real-time lab data with other data sources including EHR, claims and prescription data to help pharmaceutical teams identify and connect with physicians managing eligible patients at key decision time point in the patient journey.

    In today’s competitive pharmaceutical landscape, ensuring that physicians receive timely, relevant information about new therapies is essential. Quest’s unique combination of industry-leading deidentified lab data, enhanced with claims, prescription (Rx), and EHR insights, allows pharma teams to refine targeting, optimize engagement, and drive better patient outcomes.

  5. Computer Systems Assurance And Validation 7/22/2025

    Computer System Validation to cover all your GMP, GLP, GCP, and QA/QC software applications. CompliancePath currently has 30+ active projects globally supporting clients in CSV/CSA compliance.

  6. iMedNet eClinical 1/3/2018

    iMedNet is MedNet Solutions’ latest eClinical technology platform. It provides non-technical clinical research personnel with a fast, intuitive and cost-effective solution for building and managing their own clinical studies.

  7. Document Review Integrations And Technology Partners 6/18/2025

    At Ideagen, we're committed to empowering seamless collaboration and enhancing your document review process. Through strategic alliances with leading technology providers across the life science industry, we offer integrations that amplify the efficiency and effectiveness of your workflows.

  8. Navigate The Early Phases Of Product Development With Ease 6/16/2025

    Early Phase Experts

    As a full-service contract research organization, Southern Star Research has the knowledge, industry relationships and technical expertise to get your early-phase clinical trial up and running safely and efficiently.

    With a broad range of experience delivering Phase 1 Healthy Volunteer, First in Human, First in Patient and Phase 2 trials, we know just how important it is for your asset to succeed in the early development lifecycle. Our experienced team will help you obtain high-quality data that will appeal to future investors, meet the requirements of international regulatory bodies such as the FDA, EMA, PMDA, and Health Canada, and prepare your product for larger Phase 3 and 4 studies, partnerships, licensing, and sale.

    Whatever your clinical trial needs, we can provide a flexible, bespoke solution that will not only meet your regulatory requirements but also position your product for commercial success.

  9. Suvoda RTSM (IRT) 9/16/2025

    A centralized command center for patient randomization and drug supply management—built for today’s complex clinical trials.

  10. Commercialization And Outcomes 5/17/2018

    ICON Commercialization & Outcomes (ICO) optimizes the value of drugs and medical devices through innovative strategies and tactics that reflect evolving evidentiary, regulatory, and reimbursement requirements.