scholarly journals La responsabilidad proactiva de las Administraciones Públicas en la protección de datos personales.

Author(s):  
Aritz ROMEO RUIZ

Laburpena: Lan honen helburua da administrazio publikoak datu pertsonalen tratamenduan duen erantzukizun proaktiboaren printzipioaren analisia eskaintzea, eta ikuspegi juridikoa ematea praktikan errazago aplikatzeko. Lana lau ataletan egituratuta dago. Lehenengoan, datu pertsonalen babesa arautzen duen esparru berriaren aurkezpen orokorra egiten da; hau da, Datuak Babesteko Erregelamendu Orokorrak (EB) ezartzen duen araudi berria aurkezten da. Bigarren atala erantzukizun proaktiboari buruzkoa da, administrazio publikoek datu pertsonalak tratatzeko oinarrizko printzipio gisa. Hirugarrenak proposatzen ditu administrazio publikoek praktikan erantzukizun proaktiboaren printzipioa betetzeko kontuan har ditzaketen hainbat neurri. Azkenik, laugarren atalak gogoeta egiten du antolamendu-aldaketak egiteko beharrari buruz, Erregelamendu Orokorraren printzipioak betetzen dituztela ziurtatzeko eta herritarrek eskubideak balia ditzaten ziurtatzeko; horrez gain, aipamen berezia egiten dio datuak babesteko ordezkariaren figurari. Ondorioztatzen den ideia nagusia da garrantzitsua dela administrazio publikoek datuak babesteko politika bat diseinatzea, lehenetsita aplikatuko dena, eta ez bakarrik erantzukizun politikoak dituztenei, baizik eta sektore publikoan lan egiten duten pertsona guztiei eragingo diena. Resumen: El presente trabajo tiene como objetivo ofrecer un análisis del principio de responsabilidad proactiva en el tratamiento de datos personales por parte de la administración pública, y pretende aportar una visión jurídica para facilitar su aplicación en la práctica. El trabajo está estructurado en cuatro apartados. En el primero de ellos se presenta, en términos generales, el nuevo marco regulador de la protección de datos personales, que es consecuencia del Reglamento (UE) General de Protección de Datos. El segundo apartado está dedicado a la responsabilidad proactiva como principio básico del tratamiento de datos personales por las administraciones públicas. El tercero propone una serie de medidas que las administraciones públicas pueden tener en cuenta para cumplir con el principio de responsabilidad proactiva en la práctica. Finalmente, el apartado cuarto aporta una reflexión sobre la necesidad de introducir cambios organizacionales para asegurar el cumplimiento de los principios del Reglamento General de Protección de datos y del ejercicio de derechos por la ciudadanía, con una especial mención a la figura del delegado o delegada de protección de datos. La principal idea que se concluye es la importancia de que las administraciones públicas diseñen una política de protección de datos que se aplique por defecto, e implique, no sólo a quienes ejercen responsabilidades políticas, sino a todas las personas que trabajan en el sector público. Abstract: The present work aims to offer an analysis of the principle of proactive responsibility in the treatment of personal data by the public administration, and aims to provide a legal vision to facilitate its practical implementation. The work is structured in four sections. The first of these presents, in general terms, the new regulatory framework for the protection of personal data, which is a consequence of the General Data Protection Regulation (EU). The second section is dedicated to proactive responsibility as a basic principle of the processing of personal data by public administrations. The third proposes a series of measures that public administrations can take into account to comply with the principle of proactive responsibility in practice. Finally, the fourth section provides a reflection on the need to introduce organizational changes to ensure compliance with the principles of the General Data Protection Regulation and the exercise of rights by citizens, with special reference to the figure of the Data Protection Officer. The main idea that is concluded is the importance for public administrations to design a data protection policy that is applied by default, and involves not only those who exercise political responsibilities, but also all those who work in the public sector.

2020 ◽  
Author(s):  
Regina Becker ◽  
Adrian Thorogood ◽  
Johan Ordish ◽  
Michael J.S. Beauvais

UNSTRUCTURED Researchers must collaborate globally to rapidly respond to the COVID-19 pandemic. In Europe, the General Data Protection Regulation (GDPR) regulates the processing of personal data, including health data of value to researchers. Even during a pandemic, research still requires a legal basis for the processing of sensitive data, additional justification for its processing, and a basis for any transfer of data outside Europe. The GDPR does provide legal grounds and derogations that can support research addressing a pandemic, if the data processing activities are proportionate to the aim pursued and accompanied by suitable safeguards. During a pandemic, a public interest basis may be more promising for research than a consent basis, given the high standards set out in the GDPR. However, the GDPR leaves many aspects of the public interest basis to be determined by individual Member States, which have not fully or uniformly made use of all options. The consequence is an inconsistent legal patchwork that displays insufficient clarity and impedes joint approaches. The COVID-19 experience provides lessons for national legislatures. Responsiveness to pandemics requires clear and harmonized laws that consider the related practical challenges and support collaborative global research in the public interest.


Author(s):  
Ana Nordberg

AbstractBiobanks are essential infrastructures in current health and biomedical research. Advanced scientific research increasingly relies on processing and correlating large amounts of genetic, clinical and behavioural data. These data are particularly sensitive in nature and the risk of privacy invasion and misuse is high. The EU General Data Protection Regulation (GDPR) developed and increased harmonisation, resulting in a framework in which the specific duties and obligations of entities processing personal data—controllers and processors—were defined. Biobanks, in the exercise of their functions, assume the role of controllers and/or processors and as such need to comply with a number of complex rules. This chapter analyses these rules in the light of Article 89 GDPR, which creates safeguards and derogations relating to ‘processing for archiving purposes in the public interest, scientific or historical research purposes or statistical purposes’. It identifies key compliance challenges faced by biobanks as data controllers and processors, such as determining whether the GDPR is applicable and its intersection with other regulations; when a biobank should be considered controller and processor; and what are the main duties of biobanks as data controllers and processors and options for compliance.


10.2196/19799 ◽  
2020 ◽  
Vol 22 (8) ◽  
pp. e19799 ◽  
Author(s):  
Regina Becker ◽  
Adrian Thorogood ◽  
Johan Ordish ◽  
Michael J.S. Beauvais

Researchers must collaborate globally to rapidly respond to the COVID-19 pandemic. In Europe, the General Data Protection Regulation (GDPR) regulates the processing of personal data, including health data of value to researchers. Even during a pandemic, research still requires a legal basis for the processing of sensitive data, additional justification for its processing, and a basis for any transfer of data outside Europe. The GDPR does provide legal grounds and derogations that can support research addressing a pandemic, if the data processing activities are proportionate to the aim pursued and accompanied by suitable safeguards. During a pandemic, a public interest basis may be more promising for research than a consent basis, given the high standards set out in the GDPR. However, the GDPR leaves many aspects of the public interest basis to be determined by individual Member States, which have not fully or uniformly made use of all options. The consequence is an inconsistent legal patchwork that displays insufficient clarity and impedes joint approaches. The COVID-19 experience provides lessons for national legislatures. Responsiveness to pandemics requires clear and harmonized laws that consider the related practical challenges and support collaborative global research in the public interest.


Author(s):  
Raphaël Gellert

The main goal of this book is to provide an understanding of what is commonly referred to as “the risk-based approach to data protection”. An expression that came to the fore during the overhaul process of the EU’s General Data Protection Regulation (GDPR)—even though it can also be found in other statutes under different acceptations. At its core it consists in endowing the regulated organisation that process personal data with increased responsibility for complying with data protection mandates. Such increased compliance duties are performed through risk management tools. It addresses this topic from various perspectives. In framing the risk-based approach as the latest model of a series of regulation models, the book provides an analysis of data protection law from the perspective of regulation theory as well as risk and risk management literatures, and their mutual interlinkages. Further, it provides an overview of the policy developments that led to the adoption of such an approach, which it discusses in the light of regulation theory. It also includes various discussions pertaining to the risk-based approach’s scope and meaning, to the way it has been uptaken in statutes including key provisions such as accountability and data protection impact assessments, or to its potential and limitations. Finally, it analyses how the risk-based approach can be implemented in practice by providing technical analyses of various data protection risk management methodologies.


2021 ◽  
Vol 11 (10) ◽  
pp. 4537
Author(s):  
Christian Delgado-von-Eitzen ◽  
Luis Anido-Rifón ◽  
Manuel J. Fernández-Iglesias

Blockchain technologies are awakening in recent years the interest of different actors in various sectors and, among them, the education field, which is studying the application of these technologies to improve information traceability, accountability, and integrity, while guaranteeing its privacy, transparency, robustness, trustworthiness, and authenticity. Different interesting proposals and projects were launched and are currently being developed. Nevertheless, there are still issues not adequately addressed, such as scalability, privacy, and compliance with international regulations such as the General Data Protection Regulation in Europe. This paper analyzes the application of blockchain technologies and related challenges to issue and verify educational data and proposes an innovative solution to tackle them. The proposed model supports the issuance, storage, and verification of different types of academic information, both formal and informal, and complies with applicable regulations, protecting the privacy of users’ personal data. This proposal also addresses the scalability challenges and paves the way for a global academic certification system.


Author(s):  
Michael Veale ◽  
Reuben Binns ◽  
Lilian Edwards

Many individuals are concerned about the governance of machine learning systems and the prevention of algorithmic harms. The EU's recent General Data Protection Regulation (GDPR) has been seen as a core tool for achieving better governance of this area. While the GDPR does apply to the use of models in some limited situations, most of its provisions relate to the governance of personal data, while models have traditionally been seen as intellectual property. We present recent work from the information security literature around ‘model inversion’ and ‘membership inference’ attacks, which indicates that the process of turning training data into machine-learned systems is not one way, and demonstrate how this could lead some models to be legally classified as personal data. Taking this as a probing experiment, we explore the different rights and obligations this would trigger and their utility, and posit future directions for algorithmic governance and regulation. This article is part of the theme issue ‘Governing artificial intelligence: ethical, legal, and technical opportunities and challenges’.


2018 ◽  
Vol 25 (3) ◽  
pp. 284-307
Author(s):  
Giovanni Comandè ◽  
Giulia Schneider

Abstract Health data are the most special of the ‘special categories’ of data under Art. 9 of the General Data Protection Regulation (GDPR). The same Art. 9 GDPR prohibits, with broad exceptions, the processing of ‘data concerning health’. Our thesis is that, through data mining technologies, health data have progressively undergone a process of distancing from the healthcare sphere as far as the generation, the processing and the uses are concerned. The case study aims thus to test the endurance of the ‘special category’ of health data in the face of data mining technologies and the never-ending lifecycles of health data they feed. At a more general level of analysis, the case of health data shows that data mining techniques challenge core data protection notions, such as the distinction between sensitive and non-sensitive personal data, requiring a shift in terms of systemic perspectives that the GDPR only partly addresses.


Hypertension ◽  
2021 ◽  
Vol 77 (4) ◽  
pp. 1029-1035
Author(s):  
Antonia Vlahou ◽  
Dara Hallinan ◽  
Rolf Apweiler ◽  
Angel Argiles ◽  
Joachim Beige ◽  
...  

The General Data Protection Regulation (GDPR) became binding law in the European Union Member States in 2018, as a step toward harmonizing personal data protection legislation in the European Union. The Regulation governs almost all types of personal data processing, hence, also, those pertaining to biomedical research. The purpose of this article is to highlight the main practical issues related to data and biological sample sharing that biomedical researchers face regularly, and to specify how these are addressed in the context of GDPR, after consulting with ethics/legal experts. We identify areas in which clarifications of the GDPR are needed, particularly those related to consent requirements by study participants. Amendments should target the following: (1) restricting exceptions based on national laws and increasing harmonization, (2) confirming the concept of broad consent, and (3) defining a roadmap for secondary use of data. These changes will be achieved by acknowledged learned societies in the field taking the lead in preparing a document giving guidance for the optimal interpretation of the GDPR, which will be finalized following a period of commenting by a broad multistakeholder audience. In parallel, promoting engagement and education of the public in the relevant issues (such as different consent types or residual risk for re-identification), on both local/national and international levels, is considered critical for advancement. We hope that this article will open this broad discussion involving all major stakeholders, toward optimizing the GDPR and allowing a harmonized transnational research approach.


This new book provides an article-by-article commentary on the new EU General Data Protection Regulation. Adopted in April 2016 and applicable from May 2018, the GDPR is the centrepiece of the recent reform of the EU regulatory framework for protection of personal data. It replaces the 1995 EU Data Protection Directive and has become the most significant piece of data protection legislation anywhere in the world. This book is edited by three leading authorities and written by a team of expert specialists in the field from around the EU and representing different sectors (including academia, the EU institutions, data protection authorities, and the private sector), thus providing a pan-European analysis of the GDPR. It examines each article of the GDPR in sequential order and explains how its provisions work, thus allowing the reader to easily and quickly elucidate the meaning of individual articles. An introductory chapter provides an overview of the background to the GDPR and its place in the greater structure of EU law and human rights law. Account is also taken of closely linked legal instruments, such as the Directive on Data Protection and Law Enforcement that was adopted concurrently with the GDPR, and of the ongoing work on the proposed new E-Privacy Regulation.


Author(s):  
Yola Georgiadou ◽  
Rolf de By ◽  
Ourania Kounadi

The General Data Protection Regulation (GDPR) protects the personal data of natural persons and at the same time allows the free movement of such data within the European Union (EU). Hailed as majestic by admirers and dismissed as protectionist by critics, the Regulation is expected to have a profound impact around the world, including in the African Union (AU). For European–African consortia conducting research that may affect the privacy of African citizens, the question is ‘how to protect personal data of data subjects while at the same time ensuring a just distribution of the benefits of a global digital ecosystem?’ We use location privacy as a point of departure, because information about an individual’s location is different from other kinds of personally identifiable information. We analyse privacy at two levels, individual and cultural. Our perspective is interdisciplinary: we draw from computer science to describe three scenarios of transformation of volunteered/observed information to inferred information about a natural person and from cultural theory to distinguish four privacy cultures emerging within the EU in the wake of GDPR. We highlight recent data protection legislation in the AU and discuss factors that may accelerate or inhibit the alignment of data protection legislation in the AU with the GDPR.


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