Miranda Mourby
Biographic Data
| ID | 5190118 |
|---|---|
| NAME | Miranda Mourby |
| GIVEN NAMES | Miranda |
| FAMILY NAME | Mourby |
| SIGNATURE | MOURBY M |
| AFFILIATIONS | University of Oxford |
| ORCID | 0000-0001-9323-9413 |
| VERIFIED | Yes |
| TOTAL WORKS | 5 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 5 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2020 |
| LATEST PUBLICATION YEAR | 2024 |
| H-INDEX | 0 |
Dictionary of Privacy, Data Protection and Information Security
The Dictionary of Privacy, Data Protection and Information Security explains the complex technical terms, legal concepts, privacy management techniques, conceptual matters and vocabulary that inform public debate about privacy.\n \nThe revolutionary and pervasive influence of digital technology affects numerous disciplines and sectors of society, and concerns about its potential threats to privacy are growing. With over a thousand terms meticulou…
Contractual Mechanisms for Securing the Public Interest in Data Sharing in Public-Private Health Research Partnerships
Public private partnerships (PPPs) are increasingly common in health research, with large European investment over the last 20 years and renewed focus in the wake of the global health crisis COVID-19. PPPs have been used for health research that seeks to collect, analyse and share personal data from research participants, often on the basis of informed or broad consent. PPPs are underpinned by contracts, both to govern the use of data and samples…
Controversies between regulations of research ethics and protection of personal data: Informed consent at a cross-road
Ethical Issues in Consent for the Reuse of Data in Health Data Platforms
Data platforms represent a new paradigm for carrying out health research. In the platform model, datasets are pooled for remote access and analysis, so novel insights for developing better stratified and/or personalised medicine approaches can be derived from their integration. If the integration of diverse datasets enables development of more accurate risk indicators, prognostic factors, or better treatments and interventions, this obviates the …
Governance of research consortia: Challenges of implementing Responsible Research and Innovation within Europe
Responsible Research and Innovation (‘RRI’) is a cross-cutting priority for scientific research in the European Union and beyond. This paper considers whether the way such research is organised and delivered lends itself to the aims of RRI. We focus particularly on international consortia, which have emerged as a common model to organise large-scale, multi-disciplinary research in contemporary biomedical science. Typically, these consortia operat…
No prominent works on this page.
Governance of research consortia: Challenges of implementing Responsible Research and Innovation within Europe
Responsible Research and Innovation (‘RRI’) is a cross-cutting priority for scientific research in the European Union and beyond. This paper considers whether the way such research is organised and delivered lends itself to the aims of RRI. We focus particularly on international consortia, which have emerged as a common model to organise large-scale, multi-disciplinary research in contemporary biomedical science. Typically, these consortia operat…
Ethical Issues in Consent for the Reuse of Data in Health Data Platforms
Data platforms represent a new paradigm for carrying out health research. In the platform model, datasets are pooled for remote access and analysis, so novel insights for developing better stratified and/or personalised medicine approaches can be derived from their integration. If the integration of diverse datasets enables development of more accurate risk indicators, prognostic factors, or better treatments and interventions, this obviates the …
Controversies between regulations of research ethics and protection of personal data: Informed consent at a cross-road
Contractual Mechanisms for Securing the Public Interest in Data Sharing in Public-Private Health Research Partnerships
Public private partnerships (PPPs) are increasingly common in health research, with large European investment over the last 20 years and renewed focus in the wake of the global health crisis COVID-19. PPPs have been used for health research that seeks to collect, analyse and share personal data from research participants, often on the basis of informed or broad consent. PPPs are underpinned by contracts, both to govern the use of data and samples…
Dictionary of Privacy, Data Protection and Information Security
The Dictionary of Privacy, Data Protection and Information Security explains the complex technical terms, legal concepts, privacy management techniques, conceptual matters and vocabulary that inform public debate about privacy.\n \nThe revolutionary and pervasive influence of digital technology affects numerous disciplines and sectors of society, and concerns about its potential threats to privacy are growing. With over a thousand terms meticulou…
Ethics in Clinical Research (4 works) · Political science (4 works) · Biomedical Ethics and Regulation (3 works) · Data Protection Act 1998 (3 works) · Law (3 works) · Business (2 works) · Computer Science (2 works) · Engineering (2 works) · Engineering ethics (2 works) · Epistemology (2 works)