Medication - Sterile Compounding - Low Volume Hazardous Medication Preparation (USP 797 2008 Version Only)
Our Organization compounds a small quantity of hazardous medications. Are there any special requirements we should follow ?
Any examples are for illustrative purposes only.
Ideally, hazardous medications would be compounded in a negative pressure environment. Currently, according to USP 797, if an organization prepares a low volume of hazardous drugs, the use of two tiers of containment is acceptable in a non-negative pressure area. An example of 2-tier containment would be the use of a closed system transfer device utilized within a biological safety cabinet or compounding aseptic containment isolator.
Ideally, hazardous medications would be compounded in a negative pressure environment. Currently, according to USP 797, if an organization prepares a low volume of hazardous drugs, the use of two tiers of containment is acceptable in a non-negative pressure area. An example of 2-tier containment would be the use of a closed system transfer device utilized within a biological safety cabinet or compounding aseptic containment isolator.
Manual:
Critical Access Hospital
Chapter:
Medication Management MM
First published date: January 23, 2018
This Standards FAQ was first published on this date.
This page was last updated on November 05, 2024
with update notes of: Editorial changes only
Types of changes and an explanation of change type:
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Reflects new or updated requirements: Changes represent new or revised requirements.
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