Evidence-gap assessment
Review existing research, clarify unmet information needs, and translate broad priorities into focused questions and a proposed research scope.
Real-World Evidence · Research and analytics
Support real-world evidence (RWE) initiatives with patient and HCP insights, evidence-gap assessment, and analysis of suitable healthcare data.
We help medical and research teams understand care journeys, access barriers, and unmet needs, and identify where additional evidence could inform their next decision.
Understanding RWE
Real-world data describes health status and healthcare delivery in routine settings. Sources can include electronic health records, insurance claims, patient registries, and suitable patient-generated data. RWE is the evidence derived from analyzing these data; the FDA definition focuses on the use and potential benefits or risks of a medical product.
The source alone does not establish the strength of the evidence. The research question, study design, data quality, and analysis determine what conclusions can be supported.
Read the FDA definitions →How we support your team
Review existing research, clarify unmet information needs, and translate broad priorities into focused questions and a proposed research scope.
Explore experiences, treatment burden, support needs, and barriers through interviews, surveys, and journey research. These findings can help shape study questions and interpret the context around clinical data.
Investigate treatment decisions, referral patterns, clinical workflows, and barriers to care through research with healthcare professionals.
Assess suitable, authorized datasets for coverage, completeness, and relevance. Describe populations, patterns, and differences using methods appropriate to the data and agreed question.
Connect findings across sources into reports, visualizations, and evidence summaries, with clear methods, limitations, and implications for further research.
Define a research or analytical workstream within a broader evidence program. Responsibilities, specialist requirements, and review processes are agreed with the project team before work begins.
Potential project questions
These examples illustrate possible collaborations, rather than completed RWE studies.
Where do patients encounter delays or unmet support needs across fertility, endometriosis, or menopause care?
How do geography, affordability, and referral pathways shape access to care in a defined population?
Which patient and HCP questions remain unanswered, and what data or additional research would help address them?
Project approach
Scope and collaboration
Patient insights and market research can support an evidence program, but do not on their own establish treatment effectiveness or safety. Clinical outcome studies, causal comparisons, and regulatory submissions require a separately agreed study design and appropriate clinical, epidemiological, statistical, and regulatory expertise.
Data access, privacy, ethics review where applicable, and a suitable analytical environment are defined before any transfer or analysis. For an initial discussion, share a description of your question and available sources through our contact form.
Let's discuss your project
Tell us your question, the evidence you have, and the work your team needs.