What must be included in the verification procedure for pharmacists in compounding?

In the verification procedure for pharmacists involved in compounding, the inclusion of the correct drug, dose, form, calculations, and label is crucial for ensuring patient safety and compliance with legal and professional standards. This step serves to confirm that the compounded medication is prepared accurately according to the prescription or medication order. It addresses multiple aspects that are vital to the integrity of the compounded product, such as verifying that the right ingredients are used, that they are in the appropriate quantities, and that the final formulation meets the specifications set forth by the prescriber or regulatory guidelines.

By ensuring these elements are accurate, pharmacists can reduce the risk of medication errors that could have serious consequences for patient health. Compounding pharmacy practice demands meticulous attention to detail since compounding often involves the preparation of personalized medication tailored to individual patient needs. The verification process acts as a safeguard to uphold high-quality standards in pharmaceutical care.

Other components mentioned in the options, such as analysis of employee schedules, past compounded medications, or retention of patient records, while important in the broader context of pharmacy operations, do not directly pertain to the verification of the compounded product itself. They contribute to the overall management and quality assurance in the pharmacy but are not fundamental to the immediate safety and efficacy of the compounding