What is required for the cancer committee concerning the cancer registry data?

The requirement for the cancer committee regarding cancer registry data is to establish and implement a plan each calendar year. This is essential for ensuring that the data collected is accurate, comprehensive, and effectively utilized. By creating and implementing an annual plan, the committee can set specific goals for data collection, analysis, and quality improvement initiatives.

This approach allows for the ongoing evaluation of the cancer registry's performance and ensures that the facility meets the standards set forth by the Commission on Cancer. Regular planning also facilitates compliance with reporting requirements, enhances patient care through better data utilization, and helps in the identification of trends and areas for further research.

Conducting an annual audit, while important for quality assurance, is generally part of the larger plan and does not encapsulate the full scope of responsibilities the cancer committee must undertake yearly. Similarly, creating a new policy might be necessary, but the requirement to establish and implement a comprehensive plan encompasses broader and ongoing actions. Presenting findings to the board is a part of communication responsibilities, but it does not address the systematic approach needed to manage and utilize registry data effectively.