Clinical Platform CR+

Clinical Platform CR+ is a cloud-based clinical trials management solution developed by Circulant Solutions Inc., a life sciences IT company based in Pleasanton, California. Designed specifically for Bio-Pharma companies, the platform helps organizations manage clinical trials more effectively by centralizing data, enforcing quality controls, and enabling faster, data-driven decision-making.

The platform is built for rapid deployment — going live in less than 10 weeks — with transparent, upfront pricing. It supports FDA compliance and traceability using SAS GIT, and can be deployed to any modern cloud computing environment, offering the flexibility and scalability that evolving clinical trial needs demand.

Core Platform Capabilities

• Robust data lake architecture — Combine, store, and access clinical trials data from all sources in one secure, centralized location to drive faster decision-making.
• Embedded quality controls — Automated data quality checks are built directly into the platform to ensure the integrity of all incoming data.
• Strong access management controls — Easily define and manage access permissions for sensitive clinical trial data across teams and roles.
• Validated SAS cloud setup — A fully validated SAS environment ensures regulatory-grade reliability and compliance.
• Powerful query management platform — Create, review, and post queries within the platform or push them directly into external systems such as RAVE EDC.

Key Features

• Data Onboarder/Explorer — Upload, view, and download clinical data files through an intuitive file manager UI, or integrate with external systems via APIs for automatic data transfer.
• Data Profiler — Define and conduct automated data quality checks on all incoming data to maintain high data standards throughout the trial lifecycle.
• Rich Visualizations and Dashboards — Utilize customizable, easily configurable reports and dashboard templates built in R Shiny, Spotfire, and Power BI to generate insights and monitor clinical trials closely.
• Query Manager/Builder — Streamline query creation and management within the platform or integrate directly with EDC systems like RAVE.
• Data Mapper (SDTM) and Analytics — Convert clinical data to CDISC standards such as SDTM, and leverage analytics tools including R and SAS to perform in-depth analysis on trial data.

Deployment and Compliance

• Deployable in fewer than 10 weeks with upfront, transparent pricing.
• FDA compliance and traceability supported through SAS GIT integration.
• Compatible with any state-of-the-art cloud computing platform, ensuring scalability and flexibility.
• Designed to maximize the overall value of clinical trials by enabling faster, more informed decisions throughout the trial process.