Accelerate the development and launch of new drugs, devices, and therapies with market-leading tools and data-driven guidance. 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.
Supporting more than250Kclinical trials to date
Real-world data set with more than100Mpatients
Processing more than10Msafety cases
Industry recognition with more than1,500scientific publications
Discover solutions designed to help life sciences organizations unify data from preclinical planning, clinical trial conduct, streamlined and automated safety management, market access and brand strategy, through to post-launch performance activities, while strengthening business operations.
Data, tools, and guidance to identify and prioritize opportunities and optimize clinical trial planning.
Reduce your trial planning time by 80% and deliver accurate, on-time, and achievable forecasts based on industry benchmarks.
Use patients’ real-life experiences to strengthen clinical trial protocols and regulatory impact.
Explore Voices to Trials (PDF)
Understand progression of disease, subpopulations, and endpoints through a patient registry or cohort study.
Explore patient registries
Gain accurate, comprehensive analysis on the incidence, distribution, and control of diseases.
Leverage oncology-specific data and expertise to help you prioritize your pipeline and optimize your portfolio.
Explore oncology consulting
Access customized consulting services to inform decisions when developing treatments for rare diseases.
Explore rare disease consulting
Evaluate in/out licensing opportunities and the commercial potential for pharma assets.
Explore business development and licensing
Technology to meet the demands of today's clinical research and drug safety, ensuring innovation is at the forefront in clinical trial execution.
Improve productivity by automating and reporting on clinical trial operations data across all study management processes.
Explore Siebel Clinical Trial Management System
Select and activate sites in record time while monitoring key milestones to keep budgets and timelines on track.
Explore clinical study startup solutions
Take back control and shave weeks off your initial study build and ongoing mid-study changes.
Relieve the pressure of growing caseloads while maintaining compliance with regulations and standards by automating safety case management.
Explore Argus—safety case management
Collect data sets from any source and harmonize them in one place to draw valuable clinical insights.
Explore Clinical One Data Collection
Automatically reconcile data and maintain complete traceability with one source for clinical trial data.
Explore clinical data management
Reduce processing time by 50% while improving accuracy and compliance through AI-powered digital case intake.
Explore Safety One Intake
Insights to guide your decision-making, from strategic planning to launch optimization and beyond.
Get expert analytics and consultancy to help you optimize brand performance.
Explore brand and marketing strategy
Use evidence and insights about your market’s size, potential, dynamics, and key success factors.
Explore commercial insights
Uncover the experiences, needs, and expectations of patients, physicians, and payers.
Explore patient, physician, and payer insights
Leverage oncology-specific data, insights, and consultancy to support successful commercialization.
Explore oncology consulting
Use holistic, evidence-based consulting to guide the commercialization of treatments for rare diseases.
Explore rare disease consulting
Take advantage of evidence-based solutions to measure stakeholder perceptions of your company.
Explore corporate reputation assessment
Use readily available research and data to support market analysis and commercial decision-making.
Explore syndicated reports and insights
Shape crucial market choices and value substantiation with the depth and breadth of integrated clinical EHRs, claims, and patient reported outcome data, backed by analytical and therapy area expertise.
Get guidance and insights to develop strong value and pricing strategies for enduring treatment access.
Explore market access
Gain data and evidence for a comprehensive view of patients globally.
Explore real-world data analysis
Access expansive, proprietary databases to help demonstrate product value and differentiation.
Explore patient-reported outcomes
Automate safety signal detection with proven algorithms developed by world-class statisticians and data scientists.
Explore Empirica—safety signal management
Uncover patient insights to improve study design, support claims, and strengthen dossiers.
Explore real-world qualitative research
Identify and quantify the preferences of patients, physicians, caregivers, and payers.
Explore stakeholder preferences studies
Use observational research to define, substantiate, and communicate treatment value.
Explore non-interventional studies
Rethink the possible. Stay at the forefront of clinical research and safety solutions with our Innovation Series webinars.
Raji Modi, Senior Director, Healthcare & Life Sciences, Oracle
Renowned medical expert Sir John Bell engaged in a fascinating conversation with Oracle to discuss the challenges in improving global health outcomes. As a leading figure in the life sciences industry and Regius Professor of Medicine at Oxford University, he shared his insight on the transformative potential of new medical tools, the importance of digital advancements, and the game-changing implications of Oracle's acquisition of Cerner.
Plan resources with agility.
Build talent to propel your science.
Evolve your marketing strategy and build relationships.
Accelerate drug discovery with the cloud.
Get the latest insights and best practices to drive your clinical success.
Explore technical support contacts and resources.
Hear from thought leaders on trends in life sciences.
Contact us about clinical research and pharmacovigilance.