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Analysis of Tasimelteon in Pharmaceutical Formulations and Bulk Based on Design-Based Quality Approach by HPLC and Greenness Evaluation of the Method

dc.contributor.authorSaniye Özcan
dc.contributor.authorElif Özge Erkan
dc.contributor.orcid0000-0002-5492-0457
dc.date.accessioned2026-05-20T10:21:06Z
dc.date.issued2026-02-13
dc.identifier.doi10.1093/chromsci/bmag005
dc.identifier.issn0021-9665
dc.identifier.issue3
dc.identifier.openalexW7137143654
dc.identifier.urihttps://hdl.handle.net/11421/39822
dc.identifier.urihttps://doi.org/10.1093/chromsci/bmag005
dc.identifier.volume64
dc.language.isoen
dc.relation.ispartofJournal of Chromatographic Science
dc.rightsrestrictedAccess
dc.subjectNormalization (sociology)
dc.subjectLinearity
dc.subjectMetric (unit)
dc.subjectHigh-performance liquid chromatography
dc.subjectAccuracy and precision
dc.subjectCoefficient of determination
dc.subjectVolumetric flow rate
dc.subjectCorrelation coefficient
dc.subject.sdg15
dc.subject.sdg12
dc.titleAnalysis of Tasimelteon in Pharmaceutical Formulations and Bulk Based on Design-Based Quality Approach by HPLC and Greenness Evaluation of the Method
dspace.entity.typePublication

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