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This method quantifies everolimus residues in cleaning validation, indicating its suitability for pharmaceutical quality assurance.
The developed method provides a sensitive, precise, and eco-friendly solution for the quantification of everolimus residues in cleaning validation processes. It fulfills regulatory expectations and is suitable for routine use in pharmaceutical quality control settings, reinforcing product safety and operational efficiency.
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Gohel et al. (2026) studied this question.
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