Experience the power of fast, flexible clinical trial analytics to support clinical and operational decisions and speed promising treatments to market.
Learn how the use of FAIR Data Principles in clinical development can help you spend less time managing data and more time delivering clinical trial insights to inform clinical and operational decisions.
Connect & combine all major data sources
Centralized analytics for the entire clinical R&D lifecycle
Track data review status, collaborate, & highlight outliers
Rapidly configurable for any study or therapy
Create biomarker led trials with higher success rates
Effectively monitor trial safety, efficacy, & data quality across the entire portfolio and rapidly respond to protocol amendments.
Drive guided processes through the medical monitoring practice including safety analysis and line listing review while preventing study biasing.
Identify & communicate milestone, recruitment, site, & protocol deviation challenges to the entire team.
Better forecast challenges unique to my protocol or therapy and leverage methods available to centrally monitor my study.
Identify the best methods to identify safety signals across internal, public, and other data sets. Proactively detect safety and efficacy from real world data.
Enable researchers to identify biomarkers that allow for better cohort selection and improved patient stratification.
The Revvity Clinical analytics platform, powered by global analytics leader Spotfire™, provides a portfolio of purpose-built solutions that help improve efficiency across functional teams within Clinical Development. Our solutions support every use case, are fully customizable, and can harmonize real-time access to data from multiple sources throughout all phases of clinical development. Accessing the right data at the right time helps accelerate decisions and drive innovation from concept through trial completion and regulatory approvals, becoming an essential part of the pharmaceutical Research & Development workflow.
