PCQC is a 501(c)3 organization, led by a board of directors, that houses a new national palliative care data registry system, which will capture both program and patient-level quality data. Robust palliative care data provides insights and supports advancements in care for those with serious illness. The PCQC registry collects and collates your data, generates reports, and provides opportunities for action. Visit the PCQC's Virtual Table Chats during the Annual Assembly.