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.
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.
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.
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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.
Leading Analytical Scientists with Advanced Instrumentation.
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.
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.
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.
Efficiently and effectively manage your trip checklists to help ensure compliance during any clinical trial with iMedNet.
TrialMax Web™ is a web-based diary specifically designed for late phase trials, which tend to be larger and longer in duration.