Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/528440
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dc.coverage.spatialPharmacy
dc.date.accessioned2023-12-06T08:38:37Z-
dc.date.available2023-12-06T08:38:37Z-
dc.identifier.urihttp://hdl.handle.net/10603/528440-
dc.description.abstractquotBackground: Medical devices are the integral part of modern medical industry. The dependency of medical device has increased handsomely in treatment of diseases. This dependency has led to quality issues in medical care resulting in complications in the condition of the patients as the body does not accept them and consider them as foreign body. Therefore, for manufacturing of medical device safety and quality are given prime importance in its regulation. Initially the regulation around the world was evolving and now by introducing guidelines and policies and the revision of law has provided satisfactory guidance for the manufacturers and agencies to manufacture and check the quality appropriately. The regulation will implement the safe manufacturing, quality, and uniformity of medical devices throughout and it will also ease the importing procedures into India. The guidelines implemented and regulated effectively will have a positive outcome. newlineAim: The objective of the present study is comparison of regulatory guidelines for medical devices in India and US and European Union newlineMaterial and Methods: The research work involves study of Medical regulation of US, EU and its comparison with Indian regulation by conducting study of different class of medical devices. Data collected was analyzed for device problems and complications. The data for reporting of issues was further checked with regulatory websites of India and other countries. newlineResults and Discussion: In the study four medical devices from different classes (Class A, Class B, Class C and Class D were selected and the study was conducted in various hospitals of four towns in Gujarat. The hospitals were government and private hospitals. A total of 2323 cases were studied from four cities. Maximum numbers of patients were of urinary catheter and IV cannula. Government hospital showed more number of patients compared to private hospitals. The primary reason was the treatment in Government hospital is cheaper than private hospitals and various medical schemes of In
dc.format.extent-
dc.languageEnglish
dc.relationNo of References 114
dc.rightsuniversity
dc.titleThe comparative study on performance of selected medical devices manufactured in india and foreign countries with regulatory aspects
dc.title.alternative
dc.creator.researcherPatel, Jigna T.
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordmanufacturing import
dc.subject.keywordMedical devices
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.subject.keywordregulatory affairs
dc.subject.keywordregulatory professionals
dc.subject.keywordWorld Health Organization
dc.description.noteReferences p. 141-151
dc.contributor.guideKapupara, Pankaj
dc.publisher.placeRajkot
dc.publisher.universityRK University
dc.publisher.institutionFaculty of Pharmacy
dc.date.registered2019
dc.date.completed2023
dc.date.awarded2023
dc.format.dimensions-
dc.format.accompanyingmaterialNone
dc.source.universityUniversity
dc.type.degreePh.D.
Appears in Departments:Faculty of Pharmacy

Files in This Item:
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01_title page.pdfAttached File164.8 kBAdobe PDFView/Open
02_prelim pages.pdf876.19 kBAdobe PDFView/Open
03_table of contents.pdf19.94 kBAdobe PDFView/Open
04_abstract and graphical abstract.pdf175.78 kBAdobe PDFView/Open
05_chapter 1.pdf1.3 MBAdobe PDFView/Open
06_chapter 2.pdf106.05 kBAdobe PDFView/Open
07_chapter 3.pdf378.95 kBAdobe PDFView/Open
08_chapter 4.pdf1.45 MBAdobe PDFView/Open
09_chapter 5.pdf1.96 MBAdobe PDFView/Open
10_chapter 6.pdf172.56 kBAdobe PDFView/Open
11_annexures.pdf1.49 MBAdobe PDFView/Open
12_plagiarism report.pdf82.21 kBAdobe PDFView/Open
80_recommendation.pdf338.39 kBAdobe PDFView/Open


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