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Data Protection by Design in the E-Health Care Sector / Chapter 7 Conclusions
Data Protection by Design in the E-Health Care Sector / Chapter 7 Conclusions
Contents
Chapter
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1–22
Titelei/Inhaltsverzeichnis
1–22
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23–36
Chapter 1 Introduction
23–36
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1.1 General introductory remarks
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1.2 Research methodology and objectives
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1.3 Structure
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37–166
Chapter 2 Data protection by design: from privacy by design to Article 25 of the GDPR
37–166
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2.1 Introductory remarks
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2.2 A comparative introduction to privacy by design
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2.3 A critical analysis of privacy by design
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2.4 Deconstructing Article 25 of the GDPR
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2.4.1 Identifying the subjects
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2.4.2 Defining technical and organisational measures
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2.4.3 Understanding the state of the art and balancing the costs of implementation
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2.4.4 Evaluating the nature, scope, context and purposes of data processing
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2.4.5 Evaluating the risks posed by data processing
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2.4.6 Defining “appropriate” and “effective” criteria
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2.4.7 Identifying the time aspect of the requirement
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2.4.8 Towards the implementation of principles and rights
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2.4.9 Data protection by default
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2.5 The related provisions of the GDPR
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2.5.1 Security measures
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2.5.2 Data protection impact assessment
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2.5.3 Certification mechanisms
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2.6 A comparison between privacy and data protection by design
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2.7 Balancing the right to data protection against other rights and freedoms
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167–292
Chapter 3 Data protection and the e-health sector
167–292
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3.1 Introductory remarks
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3.2 Data protection concerns of e-health technologies
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3.3 Regulatory framework for personal health data
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3.3.1 The definition of personal health data
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3.3.1 The legal grounds for processing
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3.3.3 The relevant and applicable provisions of the GDPR
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3.4 The case study of Electronic Health Record system
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3.4.1 The state of the art of EHR
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3.4.2 The data protection framework for EHRs
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3.4.3 Cross-border interoperability issues
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3.5 Balancing the right to data protection against public health
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293–376
Chapter 4 A comparative analysis with the US legal framework
293–376
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4.1 Introductory remarks
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4.2 Overview of informational privacy in the US and the FIPS
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4.3 The US legal framework for health informational privacy and for EHRs
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4.4 Analysing the HIPAA Privacy and Security Rules
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4.4.1 General requirements
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4.4.2 The HIPAA Privacy Rule
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4.4.3 The HIPAA Security Rule
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4.5 A comparison between HIPAA and DPbD in the e-health context
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377–420
Chapter 5 Technical tools for designing data protection
377–420
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5.1 Introductory remarks
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5.2 System and software development design
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5.3 Overview of privacy engineering approaches
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5.3.1 The PRIPARE project
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5.3.2 Privacy design strategies
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5.3.3 LIDDUN methodology
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5.4 Guidance on the risk assessment framework
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5.5 Existing standards and PETs for EHR systems
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421–468
Chapter 6 Guidelines for implementing DPbD in the EHR system
421–468
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6.1 Introductory remarks
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6.2 The methodology of the set of guidelines
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6.3 Applying DPbD to an EHR system
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6.3.1 DPbD and the EHR system
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6.3.2 Technical guidelines and measures
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6.3.3 Organisational guidelines and measures
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6.4 The set of guidelines
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6.5 Notes on liability issues: possible scenarios
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469–478
Chapter 7 Conclusions
469–478
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7.1 Concluding remarks
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7.2 Open questions
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7.3 Future research
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479–526
Bibliography
479–526
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527–532
Table of Legislation and Cases
527–532
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Data Protection by Design in the E-Health Care Sector , page 469 - 478
Chapter 7 Conclusions
Autoren
Giorgia Bincoletto
DOI
doi.org/10.5771/9783748929895-469
ISBN print: 978-3-8487-8569-8
ISBN online: 978-3-7489-2989-5
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