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dc.contributor.authorMr.Revana Siddappa Devarinti-
dc.date.accessioned2026-05-16T10:52:23Z-
dc.date.available2026-05-16T10:52:23Z-
dc.date.issued2025-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2220-
dc.description.abstractABSTRACT Introduction: Adhering to Good Clinical Practice (GCP) guidelines, it is essential that personnel engaged in clinical trials and genetic research are adequately educated and trained. Clinical trial investigators bear the responsibility to protect participant privacy and prevent the unauthorized reuse of research data. Aim: This study aims to evaluate the knowledge, attitudes, and practices (KAP) of clinical trial stakeholders regarding the reuse of genetic data for future research.en_US
dc.language.isoen_USen_US
dc.publisherKLE Academy of Higher Education and Research, Belagavien_US
dc.subjectGenetic Research, Bioethics, Genetic Consent Forms, Genetic Data-Coding, and Biorepositoryen_US
dc.titleExploration of clinical trial stakeholders perspectives towards genetic research data for future useen_US
dc.typePhd Thesisen_US
Appears in Collections:Faculty of Pharmacy

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