Central Laboratories Products/Services

51. BIOGRID: The Most Effective Way To Graphically Represent Data-Driven Insights 9/28/2022

    Bioforum’s clinical research experts have developed an intuitive and easy-to-navigate analytics and visualization platform.
    BioGRID brings clinical trial data together in a clear, focused manner to drive smart decision-making processes.

52. Data Management: Turning Data Into Insights 7/31/2025

    Turning Data into Insights

    At Catalyst Flex, we understand that clean data is the foundation of successful analyses. We are an accredited Medidata Partner and certified study builders in multiple platforms.

53. Distribute, Monitor, And Exchange Study Documents With Every Site 6/12/2025

    Effortlessly distribute, monitor, and exchange study documents with every site—wherever they work, whenever they need it.

    Other tools promise site connections, but they can't deliver 100% coverage with a solution sites actually want.

    Adoption

    They claim sites use their tool…but you need sites to love it.

    Tracking

    They let you send documents…but you need to know the status of every document at every site.

    Integration

    They offer integration within their ecosystem…but you need compatibility with every site and sponsor software.

54. 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.

55. 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.

56. Regulated Document Review 3/24/2025

    Enables secure real-time document review, co-authoring, and redaction in order to shorten the document review process by up to 65%.

57. 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.

58. Signal Management Services 8/2/2024

    ProPharma has deep expertise across all signal detection and management activities, including validation, prioritization, and assessment using data from a wide range of sources that are relevant for signal detection for the individual product(s). We are also fully trained and experienced in the EudraVigilance Data Analysis System (EVDAS) functionality and can support MAHs to comply with their obligations for signal detection and management. We leverage our robust knowledge to select the most efficient and effective method(s) for each product that is compliant with legislative requirements.

59. 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.

60. End-To-End Data Management Services 8/8/2024

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