Rave Data Management

ѱ徱岹ٲ Rave Data Management solutions for clinical data management and clinical data capture eliminate complex, manual processes and deliver higher quality data for faster insights. Resulting in critical reductions in study build time, query volume, data correction rates, and reporting turnaround.

Rave Data Management solutions, running on the ̨ͼⱦ Platform, deliver interoperability between Rave EDC, eCOA, eConsent, my̨ͼⱦ, Sensor Cloud, RTSM, Imaging, Coder,?Safety Gateway?and?Clinical Data Studio.

“It is always helpful that we’re using multiple modules [from ̨ͼⱦ] and the interface between them is already there. I don’t have to worry about the backend APIs or interfaces between one system and another. It makes it just leaner and easier to use.”

C Salam Ammus, Executive Director, Clinical Data Management, Alkermes

“… Our partnership with ̨ͼⱦ has been very collaborative from a data management perspective Its made data management easier for reviewing the data, drawing out metrics, and building the forms. Its an easier platform to design.”

C Cathy Hult, Director of Data Management, PROMETRIKA

“…the ̨ͼⱦ products are very innovative and support our very complex oncology studies…”

C Vijay Chundru,Senior Director, EDC Programming Team, Global Clinical Data Operations, Jazz Pharmaceuticals

Clinical Data Capture and Management Demo

See the ̨ͼⱦ Platform’s clinical data capture and management capabilities in action. Includes eConsent, eCOA, RTSM, Sensors, Imaging, and capture of EHR data; and Clinical Data Studio with no code, drag and drop listings, and automatic generation/posting of multiple queries to enable comprehensive, aggregated data review.

Your Path to Next- Generation Clinical Data Management?

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Navigating the Frontier of Clinical Trial Data Management: Challenges and Innovations

Listen to a replay of this expert panel from Sanofi, Bayer, Daiichi Sankyo and ̨ͼⱦ as they delve into the dynamic clinical trial data management landscape. You will learn about the latest approaches and cutting-edge technologies that are now available to improve drug development and patient outcomes.

Accelerate Data Integration, Standardization, and Review

With ̨ͼⱦ Clinical Data Studio, Rave EDC data, other ̨ͼⱦ data sources, and even non-̨ͼⱦ data can be easily integrated, standardized, reviewed, and reconciled in a no/low-code environment powered by AI.

Empowering The Transformation From Clinical Data Management To Clinical Data Science: We Have The Technology!

As the clinical trial data acquisition landscape expands, the industry requires new approaches to support the rapid pace and increasing diversity of data sources. Thus, its not surprising that the focus of clinical data management teams is shifting from reactive, exhaustive data cleaning to proactive, risk-based clinical data science.

Learn how ̨ͼⱦ empowers clinical data managers to transform into clinical data scientists and become more efficient, effective, and expert.

Risk Proofing Decision-Making

Protocol requirements often involve multiple data points from different data sources to determine screening criteria and calculate endpoint measurements. Multiple methods of data collection from sources like EDC, RTSM, eCOA, and Imaging increase data silos making it harder for site staff and study teams to access clean, reliable data and reducing the ability to make effective decisions This recorded presentation uses typical protocol requirements and illustrate the value of using the ̨ͼⱦ Clinical Cloud to collect and aggregate data to drive key study conduct decisions such as screening, open-label extensions, and cycle decisions.

Adaptive Trials

Adaptive designs leverage accumulating results during a study to adapt the course of the trial and benefit both early and confirmatory studies.?

̨ͼⱦ has extensive experience with adaptive trial designs. Our multidisciplinary expert teams can help with the planning and implementation of your adaptive design, so that common challenges and pitfalls are circumvented.

Benefits of Rave Data Management

Reduced Risk

Reduce risk to data integrity, data quality and patient safety. The ̨ͼⱦ Platform delivers complete data transparency within a study or across a portfolio, empowering study teams to accelerate decision-making and drive study efficiencies, ultimately reducing risk and timelines.

Accelerated Timelines

Managing all your data on a single, unified platform improves pace and productivity.?

The ̨ͼⱦ Platform offers streamlined workflows enabling faster study build and database lock.

Agility and Flexibility

̨ͼⱦ’s platform meets the agility and flexibility needs of any trial. ̨ͼⱦ and our customers perform an average of over 30,000 mid-study changes per year, including for studies with tens of thousands of patients. The combination of our technology and experienced Professional Services team ensures smooth implementation of mid-study changes, with minimal downtime, for even the most complex, large-scale, and time-critical trials.

Simplified Integration

The ̨ͼⱦ Platform unified platform delivers full interoperability across our applications. It enables you to reduce redundancy and non-value added activities derived from data transfers, integrations and reconciliations common with disparate systems.

̨ͼⱦ also has an open integration framework and APIs enabling integration with any in-house or 3rd party system.


Rave EDC

Rave EDC is the most advanced, robust, and secure system for clinical trial site, patient, and lab data capture and management.?

Clinical Data Studio

Accelerate clinical data integration, standardization, review, and reconciliation with Clinical Data Studio.


Rave RTSM is the only fully pre-validated randomization and trial supply management solution that can be configured in minutes and enables mid-study changes with minimal downtime and no change orders.

̨ͼⱦ eCOA

̨ͼⱦ eCOA (Clinical Outcome Assessment) is revolutionizing the way sponsors, CROs, and sites collect electronic data from patients, physicians, and caregivers.?

̨ͼⱦ eConsent

ѱ徱岹ٲ eConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials.?

̨ͼⱦ Sensor Cloud

̨ͼⱦ Sensor Cloud takes a unique approach to the ingestion, standardization and scalability of data from any commercial or medical grade sensor device.


my̨ͼⱦ is a single-destination patient portal, enabling patients to virtually enroll and participate in clinical trial activities.

Rave Imaging

Rave Imaging provides cloud-based, secure management for all your medical imaging tasks in an innovative and intuitive system.

Rave Coder

Rave Coder provides medical coding for verbatim terms from Rave EDC and external sources using the MedDRA, WHODrug and JDrug dictionaries.

Rave Safety Gateway

Rave Safety Gateway delivers precise, accurate, and efficient transmission of AEs and SAEs in Rave EDC to your safety system.

Site Cloud End of Study

Site Cloud End of Study (EOS) is the first end-to-end solution that seamlessly generates, distributes & manages study files at the end of a study.

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Revolutionizing Clinical Studies with Adaptive Trial Designs

̨ͼⱦ has extensive experience with adaptive trial designs. Our multidisciplinary expert teams can help with the planning and implementation of your adaptive design, so that common challenges and pitfalls are circumvented. Discover the benefits of adaptive clinical trial designs. Maximize outcomes, efficacy, and patient safety.

NY NEXT Benefits Beyond EDC

The fireside chat will cover a pharmaceutical companys experience on the decision-making process to move to the platform and what they have learned in the process, and a CRO will describe how it has positively impacted the study build, conduct and close out processes.

Personalized Assessment Tool

What are your biggest challenges and priorities for clinical data capture and management in your studies?

Explore our interactive tool to discover how ѱ徱岹ٲ solutions can help you address your specific challenges, and receive a personalized action plan.

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