Pharmacies · Quality Control · Advanced
USP <797> sterile compounding compliance checklist covering garbing, environment, technique, BUD, and documentation.
USP General Chapter <797> establishes minimum standards for sterile compounding to prevent harm from contaminated preparations. This checklist covers the key compliance areas: cleanroom garbing and hand hygiene, environmental monitoring, aseptic technique verification, ingredient verification, beyond-use dating, and compounding documentation.
Daily documented compliance supports state board of pharmacy requirements, Joint Commission medication management standards, and protects patients from compounding errors.
This checklist template is provided as a general-purpose resource and is not tailored to the regulatory requirements of any specific country, region, or jurisdiction. It is the responsibility of each organisation to review and adapt this template to ensure compliance with all applicable local laws and regulations. Miratag does not accept liability for any inaccuracies or omissions, or for any actions taken based on this template.
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