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 |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
01_title.pdf | Attached File | 114.05 kB | Adobe PDF | View/Open |
02_prelim pages.pdf | 3.22 MB | Adobe PDF | View/Open | |
03_contents.pdf | 262.49 kB | Adobe PDF | View/Open | |
04_abstract.pdf | 439.84 kB | Adobe PDF | View/Open | |
05_chapter 1.pdf | 337.89 kB | Adobe PDF | View/Open | |
06_chapter 2.pdf | 427.65 kB | Adobe PDF | View/Open | |
07_chapter 3.pdf | 353.32 kB | Adobe PDF | View/Open | |
08_chapter 4.pdf | 170.55 kB | Adobe PDF | View/Open | |
09_chapter 5.pdf | 2.13 MB | Adobe PDF | View/Open | |
10_chapter 6.pdf | 78.21 kB | Adobe PDF | View/Open | |
11_annexures.pdf | 470.68 kB | Adobe PDF | View/Open | |
80_recommendation.pdf | 191.26 kB | Adobe PDF | View/Open |
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