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Oracle Health Sciences Clinical One unifies people, process, and data to simplify clinical trials and provide the new capabilities that are needed for the trial of today and in the future.
The only way to map a course to a better future is to understand the current landscape and what perpetuates the status quo. Insights gathered from research into clinical trials reveal the challenges and priorities that will shape the journey to the future of clinical research.
"I really wanted to hone my understanding of the issues and barriers preventing clinical research from being more efficient and effective. To do this, I needed to get out in the field." —Kathy Vandebelt, Global Head of Innovation, Oracle Health Sciences
Oracle Health Sciences helps you get therapies to market faster and detect risks earlier. Oracle offers a complete set of clinical and safety solutions that support critical processes throughout the clinical development lifecycle—from study design and startup to conduct, close-out, and post-marketing.
Oracle Health Sciences Clinical One cloud environment changes the way clinical research is done—accelerating all stages of the drug development lifecycle by eliminating redundancies, creating process efficiencies, and allowing the sharing of information across functions.
Oracle Health Sciences Data Management Workbench helps you make critical decisions fast with real-time access to complete and trustworthy trial data.
Oracle Health Sciences mHealth Connector Cloud Service enables real-time data acquisition from digital tools such as telehealth, remote patient monitoring devices, wearable technology, secure messaging, and mobile apps, delivering data directly to multiple targets all within one reusable, scalable platform.
Oracle Argus Safety Cloud Service automates business processes and workflows using artificial intelligence to increase efficiency and productivity.
Oracle Argus Safety Cloud Service provides an integrated suite of market-leading safety-case management and safety-signal management solutions, enabling unified multivigilance.
Oracle Health Sciences ClearTrial Plan and Source Cloud Service helps you plan, forecast, and outsource clinical projects quickly and accurately—saving you time and money.
Oracle Health Sciences Clinical One Randomization and Supplies Management is the first—and only—RTSM solution that gives users control and reduces study-build times from weeks to days.
Oracle Health Sciences InForm reduces trial timelines, costs, and risks via advanced EDC and query management, real-time data visibility, and standards-based, integrated workflows.
Oracle Health Sciences Data Management Workbench provides the information you need to identify and respond to trial issues early and fast.
Oracle Argus Cloud Service is the market-leading solution for processing, analyzing, and reporting adverse event cases originating in pre- and post-market drugs, biologics, vaccines, and devices. It is fully compliant with the European Medicines Agency’s enhanced EudraVigilance system.
Oracle Health Sciences executives describe the complex process of evaluating the safety and efficacy of a new drug and how advanced technology supports the collection, analysis, and reporting of trial data required to bring the drug to market.
The trials were successful…we will be using the platform again. Since we had such success the first time, why change it?Kristen Striffler, Associate Director, Clinical Development, Oyster Point Pharma
The greatest benefit of using InForm and DMW is that the systems were made for each other. From a metadata perspective, they work together.Ralph Russo, Senior Director, Database Management, Pfizer
Our top benefit with Oracle CTMS is related to trip reports. What we have seen since we have rolled it out is that our CRAs have a much more efficient turnaround time in being able to write their trip reports. So that’s a huge efficiency that we can see.Nick Poulson, Sr. Project Manager, Rho
Another big point is the ability to incorporate the third party data through the same interface. One of the top features of DMW is you now have an interface that marries up with what you’re collecting in the EDC.Demetris Zambas, Global Head of Data Monitoring and Management, Pfizer
Within a very short time, AI will revolutionize case management and signal management allowing safety departments to operate more efficiently and effectively.
Perspective from the field to fully understand the issues and barriers preventing more efficient and effective clinical research.
A truly unifed eClinical platform offers common features and functions that support multiple processes across different capabilities. It provides a single source of truth that can be used throughout the clinical trial lifecycle.