Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/418088
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DC FieldValueLanguage
dc.coverage.spatialPharmacy
dc.date.accessioned2022-11-10T09:11:48Z-
dc.date.available2022-11-10T09:11:48Z-
dc.identifier.urihttp://hdl.handle.net/10603/418088-
dc.description.abstractavailable
dc.format.extenti-xii, 1-85 p
dc.languageEnglish
dc.relation70
dc.rightsuniversity
dc.titleHarmonized technical guidance to industry and regulatory authorities for premarket and post market phase of medical devices main focus towards in vitro diagnostic medical devices ivd
dc.title.alternative
dc.creator.researcherM, Sella Senthil
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordIn-vitro Diagnostic Medical devices, stability study, Performance Evaluation, Post-Market Surveillance, COVID-19, WHO PQDx
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.description.notequotsummary p 78, References 79-83 p quot
dc.contributor.guideGowthamarajan, K
dc.publisher.placeMysore
dc.publisher.universityJSS Academy of Higher Education and Research
dc.publisher.institutionColleges of Pharmacy
dc.date.registered2018
dc.date.completed2022
dc.date.awarded2022
dc.format.dimensions3
dc.format.accompanyingmaterialCD
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:College of Pharmacy

Files in This Item:
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01_title.pdfAttached File114.05 kBAdobe PDFView/Open
02_prelim pages.pdf3.22 MBAdobe PDFView/Open
03_contents.pdf262.49 kBAdobe PDFView/Open
04_abstract.pdf439.84 kBAdobe PDFView/Open
05_chapter 1.pdf337.89 kBAdobe PDFView/Open
06_chapter 2.pdf427.65 kBAdobe PDFView/Open
07_chapter 3.pdf353.32 kBAdobe PDFView/Open
08_chapter 4.pdf170.55 kBAdobe PDFView/Open
09_chapter 5.pdf2.13 MBAdobe PDFView/Open
10_chapter 6.pdf78.21 kBAdobe PDFView/Open
11_annexures.pdf470.68 kBAdobe PDFView/Open
80_recommendation.pdf191.26 kBAdobe PDFView/Open


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