Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/418088
Title: Harmonized 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
Researcher: M, Sella Senthil
Guide(s): Gowthamarajan, K
Keywords: Clinical Pre Clinical and Health
In-vitro Diagnostic Medical devices, stability study, Performance Evaluation, Post-Market Surveillance, COVID-19, WHO PQDx
Pharmacology and Pharmacy
Pharmacology and Toxicology
University: JSS Academy of Higher Education and Research
Completed Date: 2022
Abstract: available
Pagination: i-xii, 1-85 p
URI: http://hdl.handle.net/10603/418088
Appears in Departments:College of Pharmacy

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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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