Featured Products

  1. Vault CTMS

    Vault CTMS is the only modern cloud application that makes it easy for life sciences companies to unify clinical information and processes, streamline trial management, and gain complete visibility across the trial portfolio.

  2. TrialScope Transparency Management

    Clinical trial sponsors are required by law to disclose information on their clinical trials in multiple places. These regulatory requirements continue to change as new mandated registries emerge and the scope of disclosure expands. This dynamic scenario creates a challenge for sponsors who must track and manage disclosure content that is being prepared for different registries, with different requirements.

  3. Pharmaceutical Commercial Packaging Services

    The successful commercialization of your drug requires the right packaging. At Bellwyck, our eight decades of packaging experience combined with our customized Package Smart™ solutions, GMP-compliant storage capabilities and flexible serialization options, means we know exactly what you need for your commercial packaging needs.

  4. Arcos™ Block Management System

    Minimize errors, increase productivity and keep your laboratory’s resources focused on what matters most—positive patient outcomes—with the Thermo Scientific™ Arcos™ Block Management System.

  5. Central Laboratory Solutions

    Remember the time when laboratory kits were ordered and reordered by sites faxing in pieces of paper, and laboratory reports were faxed and express mailed to investigative sites around the world? Sadly that time is still here for many central laboratory providers.

  6. Consulting

    We offer advisory services that can address commercial strategy and planning, pricing and market access, medical affairs, and risk and program management. Syneos HealthTM consulting practitioners span the entire product development and delivery continuum, adding high-value counsel and recommendations that make for more successful clinical development and brand launch success.

  7. Market Research Report: Best Practices In Study Feasibility

    This market research report has been designed to help its readers navigate the medical, clinical, logistical, and regulatory challenges associated with establishing the feasibility of a clinical trial. Stakeholders from sponsor organizations, CROs, and clinical trial sites were surveyed on their top techniques and innovations used when conducting a feasibility analysis, their awareness of feasibility analysis service providers and the frequency of their use, what percentage of clinical trials require feasibility analysis, if said analysis is typically done in-house or outsourced, and the data sources utilized and a ranking of which data sources contribute to the accuracy of the estimate.

  8. Patient & Protocol Compliance In Clinical Trials

    When a patient does not comply with the treatment regimen, the integrity of the clinical trial is at stake and patient safety is at risk.  

  9. Mobile eClinical Software: mSource

    mSource is Medrio's mobile eSource application that includes mPRO, mCapture, and mConsent. All products are native applications and are designed for use in early phase and Phase I research.

  10. Registries And Observational Studies

    UBC understands the challenges surrounding registries and other real-world data studies. Our epidemiological approach to registries and other non-interventional studies focuses on collecting relevant data to understand the natural history of the diseases for which treatments are being developed, and the real-world use of medicinal products in the post-marketing period, either as an ad hoc study, in electronic medical records, or by leveraging existing databases and registries.