What documentation is required for pharmacies that compound?

Pharmacies that engage in compounding are required to maintain detailed records of all compounded products. This requirement is essential because it ensures patient safety, quality control, and regulatory compliance. Detailed records provide a traceable history of each compounded formulation, including ingredients, quantities, dates, and patient-specific information.

Such documentation allows for the tracking of potential adverse reactions, facilitates recalls if necessary, and ensures that pharmacies follow appropriate guidelines and protocols during the compounding process. It also serves as evidence of adherence to Good Manufacturing Practices (GMP) and can be essential during inspections by regulatory authorities.

While other options may include some relevant practices, they do not encompass the comprehensive oversight needed for compounded products. Keeping records of supply orders or simply recording prescriptions filled does not fulfill the same level of requirement for compounded products. Additionally, making documentation optional would undermine the accountability and safety measures critical in the compounding process.