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West Virginia State Board of Pharmacy Sterile Compounding Inspection The information and comments obtained in the Nonsterile Compounding and Sterile Compounding Inspections are based on USP Chapters
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Step 1: Gather all necessary equipment and supplies for the sterile compounding process.
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Step 2: Prepare a clean and dedicated workspace, ensuring it meets the required standards of USP 797.
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Step 3: Put on appropriate personal protective equipment (PPE), including gloves, mask, and gown.
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Step 4: Perform hand hygiene using an antimicrobial soap or sanitizer.
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Step 5: Clean all surfaces and equipment that will be used during the compounding process.
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Step 6: Follow the aseptic technique when handling medications and sterile ingredients.
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Step 7: Calculate and measure the required amounts of each component accurately.
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Step 8: Mix or prepare the medication following the specific compounding instructions.
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Step 9: Label the final product properly with the necessary information.
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Step 10: Dispose of all waste and clean the workspace thoroughly after completing the compounding process.
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Step 11: Perform final quality checks and document the compounding process according to USP 797 guidelines.

Who needs usp 797 sterile?

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USP 797 sterile is necessary for any facility or individual involved in sterile compounding of medications.
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This includes hospitals, pharmacies, clinics, and other healthcare settings where sterile preparations are prepared.
03
Anyone who handles and prepares medications in a sterile environment needs to adhere to the guidelines outlined in USP 797 to ensure patient safety and minimize the risk of contamination.
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USP 797 sterile is a set of guidelines created by the United States Pharmacopeia to ensure the safe compounding of sterile pharmaceuticals.
Any facility or organization that compounds sterile pharmaceuticals is required to comply with USP 797 guidelines.
USP 797 sterile guidelines can be filled out by following the recommended practices for sterile compounding provided by the United States Pharmacopeia.
The purpose of USP 797 sterile guidelines is to prevent contamination and ensure the safety and efficacy of sterile pharmaceuticals.
Information such as batch numbers, expiration dates, ingredients used, and compounding procedures must be reported on USP 797 sterile documents.
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