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STERILE COMPOUNDING INSPECTION REPORT The Commonwealth of Massachusetts Executive Office of Health and Human Services Department of Public Health Bureau of Health Professions LicensureFULL Board of
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How to fill out sterile compounding inspection report

01
Step 1: Gather all necessary information and documents such as patient and medication records, standard operating procedures (SOPs), and facilities maintenance logs.
02
Step 2: Begin by filling out the basic information section of the report, including the date of the inspection, the name of the facility, and the name of the person conducting the inspection.
03
Step 3: Proceed to the inspection checklist section and go through each item on the list. Mark if the facility is compliant or non-compliant with each requirement.
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Step 4: Provide detailed explanations for any non-compliant items and suggest corrective actions that should be taken.
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Step 5: Evaluate the cleanliness and organization of the compounding area, including storage and disposal practices, and document any findings.
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Step 6: Assess the adequacy of equipment maintenance and calibration and note any deficiencies or concerns.
07
Step 7: Review the facility's training and competency assessment procedures for personnel involved in sterile compounding and note any areas of improvement.
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Step 8: Finally, summarize the overall findings and recommendations in the conclusion section of the report.
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Step 9: Submit the completed report to the appropriate regulatory body or supervisor.

Who needs sterile compounding inspection report?

01
Pharmaceutical compounding facilities
02
Hospitals and healthcare institutions
03
Pharmacies and drug manufacturers
04
Regulatory agencies
05
Quality assurance teams in healthcare settings
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Sterile compounding inspection report is a document that provides information on the inspection of facilities that compound sterile drugs.
Pharmacies and facilities that compound sterile drugs are required to file sterile compounding inspection report.
Sterile compounding inspection report can be filled out by providing detailed information on the compounding processes, facilities, and compliance with regulations.
The purpose of sterile compounding inspection report is to ensure the safety and quality of sterile drugs produced in facilities.
Information such as facility details, compounding processes, personnel qualifications, and compliance with regulations must be reported on sterile compounding inspection report.
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