The Challenge
Pharmaceutical developer needed qualitative insights from late-stage breast cancer patients regarding treatment journeys, side effect tolerances, and clinical trial accessibility barriers.
Our Approach
We collaborated with medical patient advocacy organizations and clinic networks. All patients' diagnoses were validated by clinical coordinators, and interviews were hosted via HIPAA-compliant online rooms.
Results
80 completes. 100% medical verification. 25-day fieldwork timeline.
Project Specifications
- Markets Covered: Germany, France, Spain.
- Audience Recruited: Late-stage breast cancer patients and active caregivers.
- Compliance Level: HIPAA compliant data lockers with GDPR registries audited.
- Session Format: 60-Minute qualitative video interviews (IDIs).
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