What is the term used to describe the record received at the central registry from reporting sources?

The term used to describe the record received at the central registry from reporting sources is "source record." This terminology reflects the nature of the information that has been collected and submitted by various healthcare facilities, such as hospitals or clinics, where patients are diagnosed and treated. Source records typically contain essential information about the patient's diagnosis, treatment, and demographic details, which are crucial for the registry's purpose of tracking and studying cancer statistics.

Utilizing the term "source record" emphasizes the origin of the data, highlighting that it is not the final output or compilation within the registry but rather the initial inputs received from the healthcare providers. This distinction is important for understanding the flow of information into cancer registries and the foundational role of reporting sources in cancer surveillance and research.