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Are cancer registries mandatory?

Cancer reporting has been required by California State law since 1985. All cancer professionals and facilities responsible for treating or diagnosing patients with cancer are required to report demographic, diagnostic, and treatment data to California Cancer Registry (CCR).

Why do we have cancer registry?

Cancer registries are data information systems that manage and analyze data on cancer patients and survivors. Cancer registries are maintained to ensure that health officials have accurate and timely information on cancer incidence, treatment, and survivorship.

What is the National Program of cancer registries?

The National Program of Cancer Registries (NPCR) provides financial and technical support to these central cancer registries and collects data on the occurrence of cancer; the type, extent, and location of the cancer, and the type of initial treatment.

What are the two primary responsibilities of the cancer registry?

Cancer Registrars The primary responsibilities of the cancer registrar are to collect and consolidate accurate data on cancers diagnosed and/or treated within an institution or other defined population while making important decisions related to those activities.

Is there a database for cancer patients?

The National Cancer Database (NCDB), a joint program of the Commission on Cancer (CoC) of the American College of Surgeons and the American Cancer Society, is a nationwide oncology outcomes database for more than 1,500 Commission-accredited cancer programs in the United States and Puerto Rico.

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