A complete and open, interoperable platform for health and life sciences innovation. Discover solutions designed to unify data from clinical trials, streamline and automate safety case management, generate real-world evidence from unique data sets, and guide brand strategy with commercial insights.
Life Sciences sector incubates its next growth phase
Discover solutions designed to help life sciences organizations unify data from preclinical planning, clinical trial conduct, streamlined and automated safety management, and market access and brand strategy through to post-launch performance activities—while strengthening business operations.
Clinical One RTSM can support a randomization strategy for the simplest to the most complex studies without the need for programming or coding, which eliminates the need for prolonged user acceptance testing.
The digital shift in clinical trials brings the potential to significantly improve both clinical data quality and the patient experience, while also accelerating the time it takes to get new drugs to market.
Oracle Life Sciences Technology Consulting brings together industry leading consultants with the product knowledge, hands-on experience, and direct lines of communication with Oracle Product Development and Product Support teams to ensure your product implementation, data migration, systems integration, technical training, and other initiatives are a success.
Oracle Patient Recruitment is a real-time patient identification dashboard tool that can reduce the time and effort needed to find potential patients for clinical trials. It optimizes pre-screening processes and streamlines workflow via a user-friendly design.
Oracle Life Sciences Clinical One Data Collection goes beyond electronic data capture, allowing you to collect datasets from any source and harmonize them in a single place to draw valuable clinical insight.
Oracle Life Sciences Data Management Workbench is the only clinical trial data management solution that provides a validated, trustworthy single source of truth for all trial data that automatically reconciles data discrepancies and provides complete traceability.
With Clinical One, you can build and modify studies without deployments, tickets, or downtime; collect data from anywhere and access trial insight anytime; and manage all your integrations in one place.
Oracle’s suite of study startup solutions (PDF) for starting clinical trials—through site identification, feasibility, selection, activation, and into conduct—can help get needed therapies to patients sooner.
Leverage embedded industry intelligence, clinical knowledge, and activity-based planning to optimize your clinical study planning and sourcing.
Improve productivity by streamlining, automating, and reporting on clinical trial operations data across all study management processes with Oracle’s Siebel Clinical Trial Management System (CTMS).
Quickly identify clinical trial site locations by showing trial-specific eligible patient counts from participating healthcare facilities using deidentified EHR data.
The market-leading, trusted solution for processing, analyzing, and reporting adverse event cases originating in premarket and post-market drugs, biologics, vaccines, devices, and combination products.
Oracle Life Sciences Technology Consulting brings together industry leading consultants with the product knowledge, hands-on experience, and direct lines of communication with Oracle Product Development and Product Support teams to ensure your product implementation, data migration, systems integration, technical training, and other initiatives are a success.
Oracle Life Sciences Empirica is the market-leading solution for detecting, analyzing, and managing safety signals originating in pre- and post-market drugs, biologics, vaccines, devices, and combination products.
Increasing regulatory pressure makes it vital to demonstrate drug safety, effectiveness, and post-approval utilization patterns under real-world conditions. We support your medical risk evaluation and management to help you optimize benefits and detect risks early on.
Oracle Life Sciences Safety One Intake leverages artificial intelligence to make safety case processing faster with better quality and compliance. By automatically extracting relevant information from safety source documents, manual data entry in Oracle Life Sciences Argus can be eliminated, increasing efficiency by up to 90%.
We help design and execute post-authorization safety studies (PASS) and post-authorization efficacy studies (PAES). Our solutions enable your organization to meet risk management requirements, fulfill post-marketing commitments, and establish evidence for safety and effectiveness in a real-world setting.
Gaining market access requires a deep understanding of payers and their needs, plus a strong evidence strategy. Our data and expertise can help you develop a compelling and robust value proposition that supports your approach.
Our experienced team can help you measure exactly what patients and physicians value, the attributes or outcomes that matter to them most, and the benefit and risk trade-offs they’re willing to make when deciding on a treatment.
Identifying and prioritizing opportunities—whether for new product development, indication extension, acquisition, or licensing—demands a clear understanding of market size, informed by reliable epidemiology data.
The key to effective brand communications is a strong positioning platform: the single, central idea that will become the foundation for why customers should use your brand.
Access specialized data and expertise to help navigate all stages of product development and support your success in oncology.
Oracle’s industry-leading consultants specialize in helping define, substantiate, and communicate to key stakeholders the true value of therapeutic products.
Oracle is a global leader for clinical outcomes assessments (COAs), including patient-reported outcomes (PRO) and observer-reported outcomes (ObsRO) instruments. We can help you to capture your patients’ perspectives with unmatched precision.
We use various methodologies, backed by extensive databases and secondary information, to provide meaningful insights into what drives your key stakeholders and how you can best meet their needs.
Understand how your life sciences brand is performing, optimize its potential, and fine-tune your strategies.
Due to their low occurrence and specific regulatory requirements, rare diseases present unique challenges in treatment development, evidence generation, and commercialization. We have a team with the knowledge and experience to support your decision making at all stages of product development.
Oracle Life Sciences Safety One Intake leverages artificial intelligence to make safety case processing faster with better quality and compliance. By automatically extracting relevant information from safety source documents, manual data entry in Oracle Life Sciences Argus can be eliminated, increasing efficiency by up to 90%.
Registry-based evidence has become an industry standard due to the consistent way in which the data is collected. Whether you need a disease or a product registry, we can support you.
Build powerful marketing strategies based on a comprehensive understanding of market dynamics. We provide in-depth analysis of current treatment patterns and algorithms and how they will evolve to help inform your product positioning.
Evaluate products and assess demand at all stages of product development, for more effective planning, resource allocation, and forecasting.
Oracle Analytics Cloud enables you to optimize and aggregate clinical data from various sources and get real-time clinical insights.
• Identify trends in patient data to personalize treatment and care
• Optimize drug discovery and development
Easily extend and support Oracle Life Science solutions using OCI’s highly secure APEX low-code development framework. Build, integrate, and innovate more with far less coding.
• Solve complex clinical and scientific data visualization challenges
• Enhance and enrich clinical trial management
OCI AI Services and Oracle Machine Learning can help you analyze, predict, and theorize on vast quantities of historical and real-time data.
• Proactively predict drug efficacy and safety
• Improve identification of potential clinical trial participants
Accelerate innovation via prebuilt connectivity, streamline your workflows, and use multicloud integration for a unified view of your data.
• Track clinical operations and manage documentation
• Communicate in real time with researchers
• Patient recruitment and retention
• Real-time trial monitoring
• Study design optimization
• Summarization
• Semantic similarity/coding
• Adverse event entity extraction
User assistance via natural language conversations
Highest performance, lowest cost GPU cluster technology with the largest cache for checkpointing
• RDMA cluster networking
• Nonblocking networks
• More local NVMe storage
• Voice transcription, subtitle creation, and metadata generation
• Object detection and classification in images
• Sophisticated text analysis including sentiment analysis and key phrase extraction
• Sequencing analysis
• Uncovering genetic variants
• Advancing disease understanding and management
Real-time undesirable event identification and observations from business data
Trusted, secure, and easy-to-use solutions bridge the gap between clinical research and clinical care.
Supporting more than 250Kclinical trials to date
Powering clinical research for 93%of top pharma companies
Real-world data set with more than 108Mpatients
Processing more than 10Msafety cases annually
Industry recognition via 1.5K+scientific publications in peer reviewed journals and congresses
Oracle collaborates with 400+ life sciences organizations, regulatory bodies, academic institutions, and Oracle partners via the Oracle Partner Network ecosystem.
A modernized, enterprise-ready RTSM that simplifies clinical trial execution.
AI and automation implemented across our unified pharmacovigilance portfolio
Automate randomization lists, modify distribution settings, design custom reconciliation forms, quickly define date fields, and create rules with operational data to improve trial efficiency and compliance.
Our collaboration with ObvioHealth allows rapid collection, integration and analysis of multi-source data collected from sites, patients, devices and labs.
Advanced RWD/RWE capabilities with Oracle Learning Health Network (LHN) and AI for enhanced patient diversity, recruitment, and retention
Support your entire clinical development lifecycle on a single cloud platform with high performance computing, data science tooling, and built-in security features.
Talk to a team member about Oracle solutions for life sciences.
Hear from scientists, clinicians, and industry leaders from pharma, biotech and CROs, who are driving innovation in life sciences and health.
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