Central Laboratories Products/Services

  1. Power Meets User-Centricity With Curebase EDC 8/29/2024

    Seamlessly integrated with Curebase’s ePRO/eCOA suite, our EDC enables hybrid and site-based studies that users will love and that streamline all of your data collection into a single, modern experience.

  2. End-To-End Data Management Services 7/31/2024

    Avance Clinical’s data management team has gained a world-class reputation for accuracy, precision, and quality of their biostatistics and pharmacokinetic (PK) analysis.

  3. Clinical Data Management 9/28/2022

    Bioforum’s Clinical Data Management team is fully committed to providing high-quality and reliable services using the industry’s leading technology designed for quality data capture.

  4. Data Management 3/25/2026

    In clinical research, data are everything. At inSeption Group, we understand the vital role data management plays in getting life-changing treatments to patients faster.

  5. Efficiency, Flexibility, And Speed: Building Better Clinical Trials 9/19/2023

    Zelta’s EDC has been used in more than 4,000 studies from startup to submission, across all phases, including over 500 phase 3c trials and 23 therapeutic areas.

  6. AI In Clinical Trials: Reporting/Analytics With TrialKit AI 9/9/2024

    Today’s clinical researchers need precise, timely, and reliable solutions for managing huge amounts of diverse data. TrialKit AI is here to meet this demand.

  7. Data Security Software For Life Sciences 12/10/2020

    Locate sensitive information and unusual behaviors, encrypt files, and prevent data theft.

  8. 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.

  9. 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.

  10. Biostatistics & Statistical Programming 9/28/2022

    Biostatistical services, including SAP development, statistical programming in SAS, analysis, submission-ready services and statistical reports are customized and designed specifically to meet your project requirements.