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Compounders must preserve a sturdy good quality assurance software as part of NAPRA’s Product Benchmarks for Pharmacy Compounding of Non-sterile Preparations; compounders may also consult with the USP for nonsterile preparations chapter on excellent assurance for advice on aspects to observe25. Documentation ought to involve rationale for excipient option and/or omission, references to revealed formulae (if applicable), and good quality Command parameters which may incorporate pH, mass analyses and/or organoleptic analyses25, 26.
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