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Compounders should really manage a robust excellent assurance program as Component of NAPRA’s Design Benchmarks for Pharmacy Compounding of Non-sterile Preparations; compounders might also consult with the USP for nonsterile preparations chapter on good quality assurance for guidance website on variables to observe25. Documentation ought to include things like rationale for excipient option and/or omission, references to revealed formulae (if applicable), and high-quality Management parameters which may contain pH, mass analyses and/or organoleptic analyses25, 26.

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