FULL- PIPELINE RESULT VIEWS – Access specimen data across trials, programs, and eras of research.
COMPREHENSIVE CONSENT VISIBILITY – Understand and implement in-life interventions based on detailed and codified specimen informed consent information.
AGGREGATED SPECIMEN DATA – Break the data silo barrier to unlock innovation with a single integrated solution that replaces isolated systems and inconsistent data formats.
SOFTWARE AS A SERVICE DELIVERABILITY – Save time and money with faster set-up and lower total cost of ownership.
IN-LIFE ACTIONABLE VIEWS – Identify performance issues and their impact on go/no-go decisions faster.
TRIAL DESIGN ENHANCEMENTS – Use retrospective data from previous programs to optimize new trials for better return on your investment.
COMPLIANCE WITH GLOBAL REGULATIONS – Minimize the risk of regulatory delays using industry-leading regulatory and informed consent analytics.
