Find the Patients
You're Missing
In the real world, biomarker-eligible patients are miscoded, rare disease patients go undiagnosed for years, and pre-launch populations are invisible in claims until after you need them. NorstellaLinQ was built to close that gap.
A claims record tells you a patient received a diagnosis code and a prescription. It doesn’t tell you what their physician observed, what symptoms were documented, how long they were on a prior therapy, or what the clinical rationale was for switching. That context lives in the notes, and that’s where the real patient story gets told. NorstellaLinQ links clinical notes, lab results, and treatment history across a longitudinal patient record to surface the patients your teams need to reach, with the context to act on them. Whether you’re building a pre-launch evidence base, identifying biomarker-driven populations, or mapping a complex disease journey, the signal is already in the data.
- Identify miscoded or underdiagnosed patient populations
- Surface biomarker-driven cohorts from clinical notes and lab data
- Build real-world evidence before launch, not after
- Map full disease journeys across a longitudinal patient record
