
Data Protection by Design in the E-Health Care Sector
Theoretical and Applied Perspectives- Authors:
- Series:
- Luxemburger Juristische Studien - Luxembourg Legal Studies, Volume 22
- Publisher:
- 18.11.2021
Summary
In the digital age, e-health technologies play a pivotal role in the processing of medical information. As personal health data represent sensitive information concerning a data subject, enhancing data protection and security of systems and practices has become a primary concern.
This book explores how an e-health system could be developed and how data processing activities could be carried out to apply data protection principles and requirements from the design stage. There is currently a lack of clarity and knowledge on the topic among developers, data controllers and stakeholders. The research attempts to bridge the gap between the legal and technical disciplines on DPbD by providing a set of guidelines for the implementation of the principle in the e-health care sector.
Keywords
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Bibliographic data
- Copyright year
- 2021
- Publication date
- 18.11.2021
- ISBN-Print
- 978-3-8487-8569-8
- ISBN-Online
- 978-3-7489-2989-5
- Publisher
- Nomos, Baden-Baden
- Series
- Luxemburger Juristische Studien - Luxembourg Legal Studies
- Volume
- 22
- Language
- English
- Pages
- 532
- Product type
- Book Titles
Table of contents
- Titelei/InhaltsverzeichnisPages 1 - 22 Download chapter (PDF)
- 1.1 General introductory remarks
- 1.2 Research methodology and objectives
- 1.3 Structure
- 2.1 Introductory remarks
- 2.2 A comparative introduction to privacy by design
- 2.3 A critical analysis of privacy by design
- 2.4.1 Identifying the subjects
- 2.4.2 Defining technical and organisational measures
- 2.4.3 Understanding the state of the art and balancing the costs of implementation
- 2.4.4 Evaluating the nature, scope, context and purposes of data processing
- 2.4.5 Evaluating the risks posed by data processing
- 2.4.6 Defining “appropriate” and “effective” criteria
- 2.4.7 Identifying the time aspect of the requirement
- 2.4.8 Towards the implementation of principles and rights
- 2.4.9 Data protection by default
- 2.5.1 Security measures
- 2.5.2 Data protection impact assessment
- 2.5.3 Certification mechanisms
- 2.6 A comparison between privacy and data protection by design
- 2.7 Balancing the right to data protection against other rights and freedoms
- 3.1 Introductory remarks
- 3.2 Data protection concerns of e-health technologies
- 3.3.1 The definition of personal health data
- 3.3.1 The legal grounds for processing
- 3.3.3 The relevant and applicable provisions of the GDPR
- 3.4.1 The state of the art of EHR
- 3.4.2 The data protection framework for EHRs
- 3.4.3 Cross-border interoperability issues
- 3.5 Balancing the right to data protection against public health
- 4.1 Introductory remarks
- 4.2 Overview of informational privacy in the US and the FIPS
- 4.3 The US legal framework for health informational privacy and for EHRs
- 4.4.1 General requirements
- 4.4.2 The HIPAA Privacy Rule
- 4.4.3 The HIPAA Security Rule
- 4.5 A comparison between HIPAA and DPbD in the e-health context
- 5.1 Introductory remarks
- 5.2 System and software development design
- 5.3.1 The PRIPARE project
- 5.3.2 Privacy design strategies
- 5.3.3 LIDDUN methodology
- 5.4 Guidance on the risk assessment framework
- 5.5 Existing standards and PETs for EHR systems
- 6.1 Introductory remarks
- 6.2 The methodology of the set of guidelines
- 6.3.1 DPbD and the EHR system
- 6.3.2 Technical guidelines and measures
- 6.3.3 Organisational guidelines and measures
- 6.4 The set of guidelines
- 6.5 Notes on liability issues: possible scenarios
- 7.1 Concluding remarks
- 7.2 Open questions
- 7.3 Future research
- BibliographyPages 479 - 526 Download chapter (PDF)
- Table of Legislation and CasesPages 527 - 532 Download chapter (PDF)
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