Experience the ease of a full-service electronic Clinical Outcome Assessment solution with one login, one app, one device, and one database.
Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.
Enable patients to virtually enroll and participate in clinical trial activities, using an intuitive, web-based patient portal, reducing the need for physical site visits.
Run more flexible, patient-centric trials through rapid sensor integration, data ingestion and digital biomarker discovery.
Capture, cleanse, manage and report clinical and operational data in a single data source for more efficient trial execution.
Streamline coding workflow and consolidate data, queries, and reconciliation, backed by a pioneering machine learning algorithm.
Transform your medical image management by optimizing workflows, reducing manual steps and query rates and increasing visibility across trials with technology that works with any network, any image format and any data set.
Accelerate study start, eliminate reconciliation and reduce risk with a 100-percent configurable randomization and trial supply management solution.
Automate adverse event data collection, tracking, and transmission to safety systems to reduce errors, improve safety, and shorten time.
Get rid of physical media and paper and seamlessly generate, distribute and manage site study files at the end of your study through a secure and trusted unified platform.
Manage clinical workflows and surface actionable insights so that you can complete your studies on time and on budget.
Unify content, data, and workflows in a fully configured electronic Trial Master File management system.
Manage the entire investigator grant life-cycle of your clinical trials from budget development to site budget negotiations and amendments, all with access to the industry’s largest database of clinical benchmarks and costs.
Accelerate payment cycle times for global sites, improve financial accuracy with the ability to handle complex site budgets and obtain complete visibility and transparency of the financial health of your trials.
Optimize your protocol design to reduce inefficiencies and site and patient burden.
Objectively identify the highest performing sites for your study.
Simplifies the detection of errors, trends and anomalies in study data to improve data quality and ensure patient safety.
Reduce the need for on-site document review with secure, remote monitoring of critical source documents.
Identify and manage the risks most important for your trial’s success.
Simplify and streamline the data verification process without sacrificing compliance or data quality.
Be sure you haven’t missed any data quality issues before regulatory submission.
Advanced analytics combined with our unparalleled clinical trial database are designed to enhance insights, accelerate approval and increase your probability of success.
Gain a competitive edge in trial planning and execution through our clinical trial analytics solution
Maximize pharmaceutical brand success with powerful commercial data management and insights, accelerating launch to peak.
Enable collaboration and precision in patient care by connecting to our new digital health data management ecosystem.
