Iowa Administrative Code - 08/21/2013

Pharmacy Board [657] | Agency Listing
Chapter 13 STERILE COMPOUNDING PRACTICES | Chapter Listing (Official Version - PDF format)
Rules PDF RTF Waivers
657.13.1 Purpose and scope.
657.13.2 Definitions.
657.13.3 Responsibilities.
657.13.4 Reserved
657.13.5 References required.
657.13.6 Policies and procedures.
657.13.7 Labeling requirements.
657.13.8 Record requirements.
657.13.9 Reserved
657.13.10 Microbial contamination risk levels.
657.13.11 Low-risk preparations and low-risk preparations with 12-hour or less beyond-use date.
657.13.12 Medium-risk preparations.
657.13.13 High-risk preparations.
657.13.14 Immediate-use preparations.
657.13.15 Utilization of single-dose and multiple-dose containers.
657.13.16 Utilization of proprietary bag and vial systems.
657.13.17 Reserved
657.13.18 Reserved
657.13.19 Reserved
657.13.20 Sterile preparation of hazardous drugs.
657.13.21 Reserved
657.13.22 Reserved
657.13.23 Verification of compounding accuracy and sterility.
657.13.24 Sterilization methods.
657.13.25 Media-fill testing by personnel.
657.13.26 Reserved
657.13.27 Physical environment requirements.
657.13.28 Cleaning, maintenance, and supplies.
657.13.29 Environmental monitoring requirements.
657.13.30 Reserved
657.13.31 Quality assurance (QA).
657.13.32 Patient or caregiver education and training.
657.13.33 Storage and delivery of sterile preparations.