Qualitative Data Reporting
for Regulatory Submissions
We partner with you to transform complex patient experience data into clear evidence for regulatory submission and strategic decision-making, building on insights generated through in-trial interviews and broader programs.
Clear evidence to meet your research goals
We tailor each report to meet your research objectives. Whether you need focused patient insights on meaningful change for regulatory submission or deep-dives into specific patient experiences, we customize each report to align with your goals.
Patient experience data reports typically include:
FDA/EMA guidance for patient experience data analysis and reporting
Patient perspectives brought to life through carefully selected quotations to illustrate key themes
Clear data visualizations that make complex findings accessible
Strategic insights and evidence to support internal decision-making
Clear patient-centered research
We analyze patient experience data to answer your strategic questions. Reports include robust evidence to support key findings, comparative analysis to draw out similarities and differences in patient experiences, and direct quotations.
Working in close partnership with you, we ensure your patient experience report is authentic, comprehensive, and well-evidenced—and provides you with clear insights and recommendations.
We bring you closer to patients
CLINIGMA® Explorer is an immersive tool to help you gain insights as they emerge. Whether you are interested in disease burden, treatment expectations, or treatment experiences captured during in-trial interviews, CLINIGMA® Explorer helps you understand patterns in the data in near real time.
Uncover the insights that matter most
Partner with our scientific team to transform your interview data into actionable insights or robust regulatory submissions.
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