Copertina

The European Health Data Space as a Case Study

Fuente: Wiley Open Access

Salvato in:

Dettagli Bibliografici
Autore principale:	Edward S. Dove
Natura:	Artículo Open Access
Pubblicazione:	Wiley 2024
Soggetti:	Ethics & Human Research
Accesso online:	Acceder al recurso
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!

Documenti analoghi

Reconsidering Open‐Ended Consent for Biospecimen and Health Record Research in the United States and Europe
di: Mark A. Rothstein, et al.
Pubblicazione: (2025)

Translational Bioethical Decision‐Making: Human Brain Organoids as a Case Study
di: John H. Evans
Pubblicazione: (2024)

Translational Bioethics in China: Brain‐Computer Interface Research as a Case Study
di: Haidan Chen
Pubblicazione: (2024)

Ethics in Mental Health Research with Haitian Migrants: Lessons from a Community‐Based Study in Santiago, Chile
di: Francesca McLaren, et al.
Pubblicazione: (2024)

Equitable Data Sharing in Collaborative Health Research in Sub‐Saharan Africa: A Translational Bioethics Perspective
di: Pamela Andanda, et al.
Pubblicazione: (2025)

Engaging Sub‐Saharan African Migrants in Social and Health Studies in Australia: Research and Ethical Challenges
di: Andre M. N. Renzaho, et al.
Pubblicazione: (2025)

Navigating University Openness in Research Policy Inconsistent with Indigenous Data Sovereignty: A Case Analysis
di: Molly Wick, et al.
Pubblicazione: (2024)

Ethical Issues Faced by Data Monitoring Committees: Results from an Exploratory Qualitative Study
di: Seema K. Shah, et al.
Pubblicazione: (2024)

Rapid Review of Therapy Protocols for Public Health Emergencies
di: Bruce G. Gordon, et al.
Pubblicazione: (2024)

The Ethical Case for Decentralized Clinical Trials
di: Kathryn Muyskens, et al.
Pubblicazione: (2024)

Digital Twins in Translational Research and Health Care: An Anthropological Perspective
di: Jennifer K. Wagner
Pubblicazione: (2026)

Exception from Informed Consent in Emergency Care Research: Reports from a Workshop Addressing “Edge Cases”
di: Jeremy Brown, et al.
Pubblicazione: (2025)

Expectations, Tensions, and Brokerage: A Discourse Analysis of Community Engagement with Health Research in South Africa
di: Sonja Klingberg, et al.
Pubblicazione: (2025)

The First‐ and Second‐Order Ethical Reasons Approach: The Case of Human Challenge Trials
di: Davide Battisti, et al.
Pubblicazione: (2024)

Positive and Negative Social Consequences of Participating in a Sexual‐Network Study
di: Morgan Spahnie, et al.
Pubblicazione: (2024)

Policies for the Inclusion of Pregnant Women in Research: Results from an International and a US Study
di: Anne Drapkin Lyerly, et al.
Pubblicazione: (2025)

Should Children Be Included in Human Challenge Studies?
di: Ariella Binik
Pubblicazione: (2024)

Institutional Review Board Obligations Regarding Study Funding Sufficiency
di: Holly Fernandez Lynch, et al.
Pubblicazione: (2026)

Addressing Incidental Findings in Neuroimaging Studies: Never Easy, Rarely Rescue
di: Hayden P. Nix
Pubblicazione: (2026)

Ethical Considerations for Enrolling “Invested Parties” in Large‐Scale Clinical Studies: Insights from the RECOVER Initiative
di: Kellie Owens, et al.
Pubblicazione: (2024)

Brain Organoid Research in a Post‐Dobbs World
di: Christine N. Coughlin, et al.
Pubblicazione: (2025)

What's in a Lie? How Researchers Judge the Justifiability of Deception
di: Kamiel Verbeke, et al.
Pubblicazione: (2025)

Building Ethical Foundations in Research: Adaptation of a Research Ethics Training Program for Adolescents
di: Angela K. S. Gummadi, et al.
Pubblicazione: (2025)

Research with Refugee Populations in North America: Applying the NIH Guiding Principles for Ethical Research
di: Julie M. Aultman, et al.
Pubblicazione: (2024)

Should Researchers Destroy Audio or Video Recordings?
di: David B. Resnik, et al.
Pubblicazione: (2024)

Single IRB Review and Local Context Considerations: A Scoping Review
di: Stephanie R. Morain, et al.
Pubblicazione: (2024)

Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit
di: Kyle B. Brothers, et al.
Pubblicazione: (2024)

Participant Misrepresentation in Online Focus Groups: Red Flags and Proactive Measures
di: Lesley Andrew, et al.
Pubblicazione: (2024)

Issue Information
Pubblicazione: (2024)

The Prospect of Artificial Intelligence‐Supported Ethics Review
di: Philip J. Nickel
Pubblicazione: (2024)

Bioethicists’ Perspectives on Ethical Research: Results of the “Views in Bioethics Survey”
di: Leah Pierson, et al.
Pubblicazione: (2026)

Emergency Care Research and Exception from Informed Consent: Addressing the Spectrum of Capacity for Consent
di: Neal W. Dickert, et al.
Pubblicazione: (2026)

Issue Information
Pubblicazione: (2025)

Issue Information
Pubblicazione: (2025)

Navigating Challenges with IRB Review for Community‐Engaged Research with Transgender Youth in the United States
di: Alic G. Shook, et al.
Pubblicazione: (2025)

Stakeholder Views on Novel Consent Forms for an Acute Stroke Trial
di: Candace D. Speight, et al.
Pubblicazione: (2025)

Our Theater of Anonymity
di: Sara Meeder, et al.
Pubblicazione: (2025)

Research Participant Bill of Rights: Clarifying the Role of Research Physicians
di: Mark A. Rothstein
Pubblicazione: (2025)

(Epistemic) Injustice and Resistance in Canadian Research Ethics Governance
di: Sarah Clairmont, et al.
Pubblicazione: (2025)

Natural Language Processing in Clinical Research Recruitment: A Scoping Review Enriched with Stakeholder Insights
di: Lara Bernasconi, et al.
Pubblicazione: (2025)