What must a pharmacy include in its record of every quality assurance review?

A pharmacy is required to include the date of the quality assurance review and the name and title of the individual conducting the review in its records. This requirement ensures accountability and traceability in the quality management process. By documenting who performed the review and when it took place, pharmacies can maintain a clear record of their quality assurance activities, which is essential for regulatory compliance and continuous improvement efforts.

In contrast, other options do not align with the standard practices of quality assurance documentation. While knowing the cost of medications or demographic information about patients may have relevance in certain contexts, they are not necessary components for the recording of a quality assurance review. Furthermore, documenting all previous errors could overwhelm the record-keeping system and detract from focusing on current quality improvement strategies. Thus, the essential elements for these records focus on the review's timing and the individual responsible for ensuring the review's credibility.