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USP 797US Sterile Compounding Standard CSP Ontario Branch Ontario Hospital Pharmacy Management Seminar Eric S. Castaño, MBA, Mph, FA SHP Clinical IQ, Copyright 20082016 20082015 Clinical IQs, LLC
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How to fill out usp 797-us sterile compounding

01
Read and understand the requirements of USP 797-US Sterile Compounding.
02
Ensure that you have the necessary equipment, supplies, and training to perform sterile compounding.
03
Verify that the compounding area meets the required environmental conditions.
04
Wear appropriate personal protective equipment, including gloves, gowns, masks, and goggles.
05
Follow proper hand hygiene procedures before and after compounding.
06
Clean and disinfect all surfaces and equipment before use.
07
Perform necessary calculations and measurements accurately.
08
Follow the guidelines for proper aseptic technique during compounding.
09
Label and package the compounded sterile preparations appropriately.
10
Store the compounded preparations under the recommended conditions and for the appropriate duration.
11
Regularly monitor and document the environmental conditions of the compounding area.
12
Stay updated with the latest guidelines and regulations related to USP 797-US Sterile Compounding.

Who needs usp 797-us sterile compounding?

01
Pharmacies and compounding facilities involved in sterile compounding.
02
Healthcare professionals, such as pharmacists and pharmacy technicians, who prepare sterile medications.
03
Hospitals, clinics, and healthcare facilities that administer sterile preparations to patients.
04
Research laboratories and pharmaceutical manufacturers that handle sterile compounds.
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USP 797 is a set of guidelines created by the United States Pharmacopeia to ensure the safe handling and compounding of sterile medications.
Pharmacies and healthcare facilities that handle sterile compounding are required to follow USP 797 guidelines.
USP 797 guidelines provide detailed instructions on how to properly handle and compound sterile medications.
The purpose of USP 797 is to protect patients from contamination and errors during the compounding of sterile medications.
Information such as compounding procedures, environmental monitoring results, and personnel training records must be reported.
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