Conducting a Data Protection Impact Assessment in Health Science: A Comprehensive Guide

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Standard

Conducting a Data Protection Impact Assessment in Health Science : A Comprehensive Guide. / Corrales Compagnucci, Marcelo; Dahi, Alan; Davis, Peter Alexander Earls.

I: European Health & Pharmaceutical Law Review, Bind 7, Nr. 3, 2023, s. 109-125.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Corrales Compagnucci, M, Dahi, A & Davis, PAE 2023, 'Conducting a Data Protection Impact Assessment in Health Science: A Comprehensive Guide', European Health & Pharmaceutical Law Review, bind 7, nr. 3, s. 109-125. https://doi.org/10.21552/ehpl/2023/3/5

APA

Corrales Compagnucci, M., Dahi, A., & Davis, P. A. E. (2023). Conducting a Data Protection Impact Assessment in Health Science: A Comprehensive Guide. European Health & Pharmaceutical Law Review, 7(3), 109-125. https://doi.org/10.21552/ehpl/2023/3/5

Vancouver

Corrales Compagnucci M, Dahi A, Davis PAE. Conducting a Data Protection Impact Assessment in Health Science: A Comprehensive Guide. European Health & Pharmaceutical Law Review. 2023;7(3):109-125. https://doi.org/10.21552/ehpl/2023/3/5

Author

Corrales Compagnucci, Marcelo ; Dahi, Alan ; Davis, Peter Alexander Earls. / Conducting a Data Protection Impact Assessment in Health Science : A Comprehensive Guide. I: European Health & Pharmaceutical Law Review. 2023 ; Bind 7, Nr. 3. s. 109-125.

Bibtex

@article{e74fe48ab8294f978a7e165ce18a7cad,
title = "Conducting a Data Protection Impact Assessment in Health Science: A Comprehensive Guide",
abstract = "This article provides a guide to conducting a data protection impact assessment (DPIA) for data sharing within health science research. Given the sensitivity of data in health sciences, a DPIA is vital to ensure adherence to data protection regulations and safeguard individual rights and privacy. This guide outlines the core components of a DPIA, including defining its purpose and scope, evaluating the necessity of data processing activities, gauging potential risks, and strategizing effective risk mitigation. By demystifying the DPIA process, this article empowers researchers and stakeholders to execute responsible and ethical data practices in line with the General Data Protection Regulation (GDPR) standards. Additionally, it offers practical examples, tools and resources to enhance the efficiency of conducting DPIAs in health science projects.",
author = "{Corrales Compagnucci}, Marcelo and Alan Dahi and Davis, {Peter Alexander Earls}",
year = "2023",
doi = "10.21552/ehpl/2023/3/5",
language = "English",
volume = "7",
pages = "109--125",
journal = "European Health & Pharmaceutical Law Review",
issn = "2751-398X",
publisher = "Lexxion Verlagsgesellschaft mbH",
number = "3",

}

RIS

TY - JOUR

T1 - Conducting a Data Protection Impact Assessment in Health Science

T2 - A Comprehensive Guide

AU - Corrales Compagnucci, Marcelo

AU - Dahi, Alan

AU - Davis, Peter Alexander Earls

PY - 2023

Y1 - 2023

N2 - This article provides a guide to conducting a data protection impact assessment (DPIA) for data sharing within health science research. Given the sensitivity of data in health sciences, a DPIA is vital to ensure adherence to data protection regulations and safeguard individual rights and privacy. This guide outlines the core components of a DPIA, including defining its purpose and scope, evaluating the necessity of data processing activities, gauging potential risks, and strategizing effective risk mitigation. By demystifying the DPIA process, this article empowers researchers and stakeholders to execute responsible and ethical data practices in line with the General Data Protection Regulation (GDPR) standards. Additionally, it offers practical examples, tools and resources to enhance the efficiency of conducting DPIAs in health science projects.

AB - This article provides a guide to conducting a data protection impact assessment (DPIA) for data sharing within health science research. Given the sensitivity of data in health sciences, a DPIA is vital to ensure adherence to data protection regulations and safeguard individual rights and privacy. This guide outlines the core components of a DPIA, including defining its purpose and scope, evaluating the necessity of data processing activities, gauging potential risks, and strategizing effective risk mitigation. By demystifying the DPIA process, this article empowers researchers and stakeholders to execute responsible and ethical data practices in line with the General Data Protection Regulation (GDPR) standards. Additionally, it offers practical examples, tools and resources to enhance the efficiency of conducting DPIAs in health science projects.

U2 - 10.21552/ehpl/2023/3/5

DO - 10.21552/ehpl/2023/3/5

M3 - Journal article

VL - 7

SP - 109

EP - 125

JO - European Health & Pharmaceutical Law Review

JF - European Health & Pharmaceutical Law Review

SN - 2751-398X

IS - 3

ER -

ID: 366893765