Featured Products

  1. CRO Project Management

    For over two decades, SynteractHCR has successfully managed over 3400 projects in multiple therapeutic areas and are proud to have supported numerous global product approvals. In addition, our specialized expertise in working with emerging pharma, biotech and device companies helps us guide them through the clinical development process.

  2. Patient Engagement

    With 50 years of serving sponsors, CROs, institutions and sites, we understand the investments behind getting your study to firstpatient first-visit as quickly and efficiently as possible. We also know one of the biggest challenges is still ahead: industry research shows that 20-25% of studies close because they fail to meet enrollment targets.

  3. Rave® EDC

    Leading and specialty CROs across the industry use Rave with their clients. Medidata's industry-leading Services Partner program helps CROs bring the best technology to their clinical development activities.

    Rave is:

    • Flexible. Don’t twist your processes to fit technology limitations.  Rave flexibility accommodates your workflow requirements.  Make mid-study changes—including adaptive trials, protocol amendments and updated requirements—easily with no system downtime. Rave manages multiple case report form (CRF) editions and seamlessly migrates existing data into new forms and structures.
    • Scalable. Rave’s cloud-native architecture scales from one study to hundreds, and from Phase-I all the way to global Phase-IV. Whatever your trial phase or business growth, one cloud system is all you need.
    • Configurable. Simple or complex study requirements, Rave handles them all without custom programming. Easily configure CRFs, workflows, data blinding, source document verification (SDV) requirements, dictionary coding and more. All via a point-and-click browser interface.

    (Please scroll down to access white papers, case studies and data sheets.)

  4. Intralinks For Clinical Operations

    Successfully manage your clinical development programs.
    Our security and governance capabilities, including ISO 207001 certification, FDA 21 CFR Part 11 validation and HIPAA compliance, were designed to protect high-value information for the most-regulated industries.

  5. Biologics / Large Molecule Analytical Services

    Leading Analytical Scientists with Advanced Instrumentation.

  6. Prancer Randomization & Trial Supply Management

    Our team has extensive experience developing complex randomization schemes, including dynamic allocation (adaptive randomization).

    Prancer supports central randomization, site blocked randomization, multiple strata, dynamically blocked to strata, dynamically blocked to strata and site as well as multiple randomizations.

  7. goBalto Analyze

    If you use goBalto Activate for study startup, you have a wealth of data for sites, study countries, and study document and submission activities that you can use in reports and analytics.

  8. Harness Real-Time Data To Optimize Clinical Trial Investigator And Site Recruitment

    Time and again, when we ask our partners in clinical development roles what their number one concern is, they respond that recruiting clinical trial patients and sites on-time and on-budget is an enormous and expensive challenge.

  9. Monitoring Trip Checklist

    Efficiently and effectively manage your trip checklists to help ensure compliance during any clinical trial with iMedNet.

  10. TrialMax Web™ eCOA (Electronic Clinical Outcomes Assessments)

    TrialMax Web™ is a web-based diary specifically designed for late phase trials, which tend to be larger and longer in duration.