For Life Sciences Companies
Aspire. Assess. Achieve.
Accelerate research with better data and analytics.
Our experience and expertise help Life Sciences organizations leverage insights from the leading patient-level data set available.
Faster patient enrollment at Cancer Center Research Consortium sites.
%
Faster feasibility—completed in 3 days, compared to 10 days for non-Consortium sites.
%
Faster activation times—completed in 86 days, compared to 147 days for non-Consortium sites.
Analytics and Answers
Dramatically reduce barriers to effective and efficient Real World Evidence-based research through analyses and insights provided by our experts.
- Benchmark Studies
- Clinical Trial Portfolio Gap Analysis
- Custom Patient Population Analyses
- Enriched Patient Datasets and External Comparators
- HEOR Modeling Support
- Landscape Analysis/Charts
- Patients on Trial vs. Standard of Care
- Retrospective Studies
- Treatment Pathways and Standard-Of-Care Analyses
Study Support
Services and access to Cancer Center Research Consortium-wide data dramatically reduce enrollment times.
- Draft Protocol Review
- Feasibility Assessments
- Inteliquet Consortium Site Selection
- Patient Identification
- Patient Matching and Screening
- Cohort Identification
- Reporting and Screening Logs
- Site Recruitment Metrics
Analytics and Answers
Dramatically reduce barriers to effective and efficient Real World Evidence-based research through analyses and insights provided by our experts.
- Benchmark Studies
- Clinical Trial Portfolio Gap Analysis
- Custom Patient Population Analyses
- Enriched Patient Datasets and External Comparators
- HEOR Modeling Support
- Landscape Analysis/Charts
- Patients on Trial vs. Standard of Care
- Retrospective Studies
- Treatment Pathways and Standard-Of-Care Analyses
Study Support
Services and access to Consortium-wide data dramatically reduce enrollment times.
- Draft Protocol Review
- Feasibility Assessments
- Inteliquet Consortium Site Selection
- Patient Identification
- Patient Matching and Screening
- Cohort Identification
- Reporting and Screening Logs
- Site Recruitment Metrics
Data
Specialists in the data available through the Cancer Center Research Consortium assist you in accessing insights to meet your needs and budget.
- De-identified
- Structured and unstructured
- EMR and related data including LIMs, Registries, PACs, or file-based system
- Multi-variate analysis behind firewalls
- Normalized across Consortium
- Custom data transfers
Enterprise Software
Inteliquery’s front-end tools give research sponsors fast, accurate access and analysis of Inteliquet Center Cancer Research Consortium data.
- Inteliquery for Life Sciences – Deidentified clinical trial patient identification
- Inteliscreen for Life Sciences – Deidentified clinical trial patient screening
- SaaS Licenses
- Query by Diagnoses, Treatments, Diagnostics, Demographics and More
- Create Trial Watch Lists
- Custom Reporting
Data
Specialists in the data available through the Cancer Center Research Consortium assist you in accessing insights to meet your needs and budget.
- De-identified
- Structured and unstructured
- EMR and related data including LIMs, Registries, PACs, or file-based system
- Multi-variate analysis behind firewalls
- Normalized across Consortium
- Custom data transfers
Enterprise Software
Inteliquery™’s front-end tools enable efficient access and analysis of EMR+ data.
- Inteliquery™–Clinical trial patient identification
- Inteliscreen™–Clinical trial patient screening
- SaaS Licenses
- Populated by Provider EMR and Unstructured Data
- Query by Diagnoses, Treatments, Diagnostics, Demographics and More
- Faster and More Accurate Analyses
- Create Trial Watch Lists
- Custom Reporting
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and contract research services to the life sciences industry dedicated to delivering actionable insights. Learn more at www.iqvia.com.
