Final answer:
Both Master Formulation Records (MFRs) and Compounding Records (CRs) are required per the 2008 version of USP 797.
Step-by-step explanation:
The 2008 version of USP 797, which stands for United States Pharmacopeia Chapter 797, is a set of guidelines that provides standards for compounding sterile preparations in healthcare settings. According to these guidelines, both Master Formulation Records (MFRs) and Compounding Records (CRs) are required.
MFRs are detailed documents that outline the formulation and compounding process for a specific drug or preparation. They contain information such as ingredients, quantities, and procedures to ensure consistent compounding practices.
On the other hand, CRs are records that document the actual compounding process for each individual preparation. They include information about the specific medication, compounding personnel, equipment used, and any relevant quality control measures.