Data Insights and Evidence Generation
Transform Data Into
Actionable Insights
Our Insights and Evidence Generation team partners with sponsors to turn complex patient, site, and trial data into clear decisions.
We generate fit-for-purpose evidence, translate findings into practical recommendations, and support implementation so teams can act with confidence.
Result: Stronger study design, better recruitment and retention, and a more patient-centered clinical trial experience.
We Bring The Patient Voice Into Drug Development
Patient-reported outcomes (PROs) capture what matters most—directly from patients. We help you design and implement PRO strategies that are scientifically robust, feasible for sites and patients, and positioned to support regulatory and access conversations.
From endpoint selection through analysis and interpretation, we focus on evidence you can defend—so stakeholders can use it to make decisions. How we support your PRO strategy:
We support.
PRO Selection & Validation. Select, justify, and refine the right PRO measures for your target population and intended claim(s).
Psychometric Testing. Evaluate reliability, validity, responsiveness, and meaningful change to confirm instruments are scientifically sound and submission-ready.
Why it matters.
Fit-for-purpose PROs. Reduce uncertainty, strengthen the patient-centered evidence story, and help teams make better decisions across development.
Why Partner
With Us?
Optimize Clinical Trial Success
Improve protocol feasibility, patient experience, recruitment, and retention so studies enroll faster and run with less avoidable variability.
Navigate Market and Regulatory Hurdles
Build defensible evidence packages aligned to regulatory expectations—and support value communication with payers and other stakeholders.
Address Patient Needs With Precision
Identify and reduce patient and site burden (time, travel, complexity, digital friction) to strengthen engagement and adherence.
Build Trust and Strengthen Reputation
Demonstrate credibility with patients, sites, and communities through transparent methods, high-quality measurement, and evidence you can explain clearly.
Access World-Class Expertise
Work with an interdisciplinary team (measurement science, qualitative research, statistics, clinical operations, and implementation) experienced in translating insights into action.
Collaborate With a Dedicated Team
Partner with a responsive team that brings structure, pace, and clear communication—so recommendations are actionable and easier to implement across stakeholders.
Case Studies: Driving
Meaningful Change
in Clinical Trials
Improving HIV Prevention
With Smarter
Implementation
The Challenge. Despite the effectiveness of HIV PrEP, uptake and persistence remain uneven—especially in populations facing access, stigma, and logistical barriers.
Our Solution. We ran a rigorous, multi-study program to compare implementation pathways (e.g., pharmacy-based delivery vs. routine care), quantify barriers, and identify scalable strategies to increase uptake and persistence.
The Impact. The findings informed practical implementation approaches—helping programs target resources where they have the greatest impact and improving the likelihood that eligible patients start and stay on therapy.
Revolutionizing Transplant
Decision-Making
The Challenge. Thousands of highly sensitized kidney disease patients face long waits—or are removed from transplant lists—due to limited compatible donor options and complex decision pathways.
Our Solution. We conducted a patient preference decision study to quantify trade-offs patients are willing to make, develop decision-support tools for shared decision-making, and identify levers to expand access.
The Impact. This work generated actionable evidence to inform program design and decision pathways, supporting more equitable access for patients disadvantaged by compatibility constraints.
Breaking Barriers in
Cancer Clinical Trials
The Challenge. Research in France and Spain showed participation skewed toward patients with stronger financial resources—highlighting barriers that limit access for underserved groups.
Our Solution. We conducted in-depth patient interviews to identify practical support needs (e.g., travel, scheduling, caregiver support, information clarity) and translate them into trial-design and operational recommendations.
The Impact. The findings informed more inclusive study designs and site-level support approaches—helping sponsors reduce avoidable barriers and improve equitable participation.
Ready to See How Data Can
Change Lives?
Contact our team to explore how evidence generation and patient-centered insights can strengthen your trial strategy and execution.
Contact Us