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/20:51:31

20:51:31Compounding Practices

Chapter · Administrative Rules of South Dakota · View on sdlegislature.gov ↗

Rulemaking activity

South Dakota Board of PharmacyFiled with SOS

Sections (37)

20:51:31:01Definitions.
20:51:31:02Standards and procedures.
20:51:31:03Manual required.
20:51:31:04Physical environment requirements for sterile products.
20:51:31:05Requirement for primary engineering control device or room.
20:51:31:06Placement of primary engineering control device.
20:51:31:07Compounding aseptic isolator (CAI).
20:51:31:08Exception for placement of CAI.
20:51:31:09Ante area requirements.
20:51:31:10Delayed implementation.
20:51:31:11Cleaning, maintenance, and supplies.
20:51:31:12Additional records required.
20:51:31:13Quality assurance.
20:51:31:14Pharmacist responsibilities.
20:51:31:15Training documentation.
20:51:31:16Reference requirements.
20:51:31:17Labeling requirements.
20:51:31:18Microbial contamination risk levels.
20:51:31:19Low-risk preparations.
20:51:31:20Medium-risk preparations.
20:51:31:21High-risk preparations.
20:51:31:22Immediate-use preparations.
20:51:31:23Utilization of single-dose and multiple-dose containers.
20:51:31:24Utilization of proprietary bag and vial systems.
20:51:31:25Sterilization methods.
20:51:31:26Media-fill testing by personnel.
20:51:31:27Environmental monitoring requirements.
20:51:31:28Storage and delivery of sterile preparations.
20:51:31:29Additional requirements for preparation of hazardous drugs.
20:51:31:30Responsibilities for patient care.
20:51:31:31Patient or caregiver education and training.
20:51:31:32Compounding and hazardous drug handling standards -- United States Pharmacopeia compounding standards implemented by reference.
20:51:31:33Policy and procedure manual.
20:51:31:34Compounding requirements.
20:51:31:35Delivery to patients.
20:51:31:36Disposal of pharmaceutical hazardous waste.
20:51:31:37Quality assurance.