Clinical Analytics
Comprehensive analytics for optimized data review & operational insights
Clinical analytics software that delivers insights across all your data
More than 50 Life Sciences companies rely on Clinical Analytics from elluminate® to improve the clinical data review process and enhance operational oversight.
Clinical Analytics Software That Makes Data Meaningful
Many R&D teams still rely on manual Excel trackers and line listings to review patient data and monitor the progress of trials. elluminate Clinical Data Analytics help you change the paradigm by transforming the data from all your sources into insights and actions for data management, medical monitoring and clinical trial operations.
- Review data faster with 30+ out of the box visualizations across 12 standard domains
- Make medical monitoring easier with oncology-specific visualizations including Hy’s Law & Tumor Response
- Visualizations combined with issue workflow and management streamline data review
Clinical Trial Analytics that Answer Your Operational Questions
To effectively manage trials according to regulatory guidance, clinical operations teams need to know the latest patient recruitment statistics along with protocol deviation numbers, screen fail rates, biomarker results and other key metrics. elluminate Clinical Trial Analytics eliminate data discrepancies from various systems by combining all your data sources. You gain one source of truth to answer your operational questions.
- 20+ trial operational visualizations for more effective trial management
- Instant insights about enrollment, data quality at sites and visit timelines
- Self-service data analyses and report creation combined with issue tracking and workflow to document oversight
- Flexible analytics architecture to solve trial management challenges including biomarker sample tracking, endpoint analyses and cross trial analyses
We were able to see that outlier just pop right out of the graphic
We had a particular piece of lab data that is difficult to review in tabular format, and were able to format the data to be pushed into a labs over time graphic. When we took that data that had been reviewed many times in tabular format and pushed it into a graphical view, we were able to see that outlier just pop right out of the graphic.
Sean McNiff,
Associate Director, Clinical Programming, bluebird bio
elluminate implementation
The elluminate implementation team focuses on ensuring clients maximize the value of their clinical trial software investment quickly. Consultants use in-depth drug development knowledge and clinical data analytics expertise to facilitate elluminate rollout, training and adoption.
Frequently Asked Questions
This sounds too good to be true, does this really work?
Yes, it does! Let us show you how in an elluminate demonstration.
How expensive is this?
elluminate is a cost-effective SAAS product and typically includes a monthly user license fee, support and an initial implementation and setup fee. There is a comprehensive set of training courses included along with 24×7 end user support. elluminate delivers value to clients by providing increased control over, and direct access to, all of the data from disparate sources being collected in clinical trials. End users who were formerly disintermediated from their data and had to rely on clinical programming teams for high quality analyses and reporting gain self-service access to curated data sets, saving both time and money. A detailed ROI model is available demonstrating how elluminate saves costs based on the products utilized and the number of ongoing and archived studies included.
Is this truly self service?
The elluminate platform is dedicated to providing clinical researchers with self-service access to their data and self-service is one of the key themes used to govern elluminate product development prioritization. In Analytics, end users can copy and save worksheets to explore data and even create their own app from a variety of different data sources, according to their permissions. elluminate enables clients to determine the types of data access and permissions that are provided to different types of users, roles and groups to ensure the organization’s optimal level of self-service access to different data stores and analytics.
Will this work with my existing platforms?
elluminate is a flexible platform that fits within existing clinical technology ecosystems. As a clinical data hub, elluminate is designed for rapid data integration. elluminate gracefully coexists with many other eclinical platforms and has an out of the box, two-way integration with the Medidata Clinical Cloud. Data from many other systems including MDR, EDC, safety, eCOA, IVR, Labs, Omics, Biomarkers, eSource and physiological sensors have been successfully integrated into elluminate. Clients can also leverage elluminate for external data sources and combine that with EDC data for analytics and review, as well as data exploration and curation via Mapper.
Will it scale?
elluminate scales effectively and leverages cloud-based processing power to ensure high performance for users independent of the volume of studies or the number of users accessing the system. elluminate uses a modern technology stack to ensure users experience optimized performance and visibility to their clinical data at all times.
Will we be able to get immediate value out of this?
Yes. As a cloud based system, elluminate can be deployed rapidly to ensure maximum value. The typical implementation and rollout takes a phased approach by identifying key value drivers elluminate can deliver for specific roles and functions, and implementing the platform to those groups while measuring success and satisfaction in the process. The goal of the elluminate delivery team is ensuring clinical teams achieve their business goals with high volume and adoption in the least amount of time.
How long will implementation take?
elluminate’s cloud-based products are designed for rapid implementation. A typical elluminate implementation takes 90 days which may include putting archived, new or ongoing studies into the hub. The implementation process includes defining the key value drivers of the system for the client, the data sources that will be included, and preparing and standardizing data. elluminate includes a validation accelerator package that provides a risk-based approach, as well as test scripts and documentation to facilitate the internal validation process. Implementation consultants guide client teams through the process, focusing on the capabilities that will maximize value to client stakeholder groups. End users are fully trained and prepared for elluminate adoption and rollout.
Is it hard to use?
elluminate is easy to use and is designed with the workflow of data management, clinical operations, and medical review of biostatistics in mind. The primary objective of elluminate Mapper is to make data integration and mapping easier for non-programmers. Data Central is designed for significantly more efficient and automated data review by data managers and medical monitors. The visualizations in elluminate Clinical Analytics are intuitive and flexible, linking to issue workflow so teams can act upon data insights in real-time. The eCS professional services team uses elluminate on every engagement to deliver high quality data services to clients, and internal power users provide continuous feedback and suggestions so that enhancements always have end user goals in mind. elluminate includes role-based training guides and videos along with best practices to ensure users are up to speed quickly.
Is this proven?
elluminate is a proven platform that has been used by Life Sciences companies since 2012. Currently, more than 50 clinical development organizations of all sizes rely on elluminate to regain control of their clinical trial data. Critical data assets across thousands of studies are currently being stored in the elluminate platform for both ongoing and archived studies, providing researchers with new clinical and operational insights. Studies using elluminate for clinical data review, management and analysis have been submitted to regulatory authorities and approved, and SDTM data that was produced with elluminate Mapper has been used for FDA submission.
How do I know it is it compliant and secure?
elluminate is fully compliant with 21CFR Part 11 and ensures data privacy and security in accordance with global regulatory requirements. elluminate has a flexible permission architecture allowing limited access to certain types of data as required per client SOP. As a proven system in use for clinical data since 2012, elluminate has been used to prepare data for numerous regulatory submissions that have received approval across therapeutic areas.
Will people actually use it?
End users from Clinical Operations, Data Management, Medical Monitoring, Biostatistics and Clinical Programming enjoy working in elluminate as it provides them with immediate value, time savings and streamlined workflows. elluminate provides clinical teams with one source of truth from which to work, eliminating the need for numerous excel trackers that tell different stories and require rework and reconciliation. The eCS Data Services team user elluminate across all client trials. elluminate is designed for maximum ease of use by clinical teams.