A quality by design approach for development optimization and validation of stability indicating method for impurity profiling and estimation of assay in selected pharmaceutical compounds by rp hplc

dc.contributor.guideVijaya Rachel, K
dc.creator.researcherSanthi Priya, Lankalapalli
dc.date.accessioned2025-07-17T06:24:35Z
dc.date.available2025-07-17T06:24:35Z
dc.date.awarded2025
dc.date.completed2025
dc.description.abstractFile Attached newline
dc.format.accompanyingmaterialNone
dc.identifier.researcherid0009-0008-8120-6444
dc.identifier.urihttp://hdl.handle.net/10603/652700
dc.languageEnglish
dc.publisher.institutionDepartment of Biochemistry
dc.publisher.placeVisakhapatnam
dc.publisher.universityGITAM University
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordBiochemistry and Molecular Biology
dc.subject.keywordBiology and Biochemistry
dc.subject.keywordLife Sciences
dc.titleA quality by design approach for development optimization and validation of stability indicating method for impurity profiling and estimation of assay in selected pharmaceutical compounds by rp hplc
dc.type.degreePh.D.

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