Welcome to the National Palliative Care Registry™

Building a profile of palliative care teams, operations and service delivery. The Registry is FREE and open to all palliative care programs across the continuum of care.

  • Palliative Care
  • Service Settings
  • Initial Patient Consultations
Since 2012

  • In Summer 2020, the Registry is moving to the Palliative Care Quality Collaborative (PCQC)!
    (Learn more)
  • Important Announcement about the Future of the Registry!
    (Read here)

Participate in the Registryhospital-icon (1)

Every program needs a plan for measuring and monitoring impact to improve quality, secure influence and garner support. Using the National Palliative Care Registry™, palliative care programs can measure their progress and track their operational capacity and reach.

Participating programs have access to a variety of reports including longitudinal data and comparison reports for peer service settings.

Sign In to the Registry

Are you new to the Registry?

CAPC membership is not required for participation.


Learn more about the Registry.

Access Metrics & Resourcesgraph-head-icon (1)

Standardization depends on clear definitions and shared goals. Metrics & Resources is a space that centralizes data resources, metrics and recent research on the operational features of palliative care programs.

Find key palliative care metrics and definitions and review findings from recently published research in the field. Download Registry summary data reports, presentations and webinars.

  • Capture-e1453314224147
    Getting the Most Out of the National Palliative Care Registry™


  • TN-2014-Annual-Survey-Summary
    National Palliative Care Registry™ 2014 Annual Survey Summary