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 NON HAZARDOUS STERILE PREPARATION ASSESSMENT CRITERIA 2021-2025

Ocp Assessment Criteria 2021-2025 Form

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sterile compounding background most parenteral formulas must be sterile meaning the formulation is free from microorganisms sterilization applies to all injectable formulations ophthalmic formulations inhalation formulations nasal aerosol formulations parenteral products have special requirements for how they are prepared packaged and admitted surgery these formulations must be sterile because they have rapid access to the circulatory system and can cause great harm compounding regulations compounding provides for patient care in multiple settings develops chemical and medical processes and protocols to provide safe medications for patients compounding regulations standards and guidelines involve the work of many organizations boards and agencies at both federal and state levels there are two primary regulators in compounding one Food and Drug Administration two individual state boards of Pharmacy the United States pharmacopoeia and National formulary USP and F has been the predominant

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