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Chapter 21-4.1.0 - Design Requirements for Compounded ...

Oct 31, 2017 Chapter - Design Requirements FOR Compounded sterile AND HAZARDOUS DRUG PREPARATION AREAS 1 A. Purpose .. 1 B. Scope .. 1 C. Background .. 1 D. Definitions .. 2 4 A. General Design Criteria for facilities .. 4 B. Design Criteria for facilities using BSCs and LAFWs .. 6 C. Design Criteria for facilities using CAIs and CACIs .. 6 D. Typical room Layouts .. 7 Tables: Construction Guidelines for Pharmacy compounding 8 Table 1: Requirements Common to All Locations and Compounded Pharmaceuticals .. 8 Table 2A: Standard Requirements for Low and Medium Risk CSPs.

defined in USP 797-2008, the buffer room shall be ... The rooms used for compounding sterile and hazardous drug preparations shall comply with the design recommendations ... Chapter 21-4.1.0 - Design Requirements for Compounded Sterile and Hazardous Drug Preparation Areas ...

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