Lista de obras - Mark Sheehan - Dominio Público Uruguay

'It's a tough decision': a qualitative study of proxy decision-making for research involving adults who lack capacity to consent in UK

artículo científico publicado en 2019

'There's more to life than money and health': Family caregivers' views on the role of Power of Attorney in proxy decisions about research participation for people living with dementia

scientific article published on 25 October 2019

'Your country needs you': the ethics of allocating staff to high-risk clinical roles in the management of patients with COVID-19

artículo científico publicado en 2020

Assent is not consent.

artículo científico publicado en 2012

Authority and the Future of Consent in Population-Level Biomedical Research

artículo científico publicado en 2019

Broad consent is informed consent

artículo científico publicado en 2011

Can Broad Consent be Informed Consent?

artículo científico publicado en 2011

Commissioning ethically and legally: the more things change, the more they stay the same.

artículo científico publicado en 2013

Constructing authentic decisions: proxy decision making for research involving adults who lack capacity to consent

artículo científico publicado en 2020

Delia Smith and the ethics committee.

artículo científico publicado en 2011

Developing a new justification for assent

artículo científico publicado en 2016

Disclosing clinical trial results: publicity, significance and independence

artículo científico publicado en 2009

Do we need research ethics committees?

artículo científico publicado en 2013

Emergency medicine research: rites, rituals and consent.

artículo científico publicado en 2013

Ethical review and ethical behaviour.

artículo científico publicado en 2005

Ethical understandings of proxy decision making for research involving adults lacking capacity: A systematic review (framework synthesis) of empirical research

artículo científico publicado en 2018

Ethics and opportunity costs: have NICE grasped the ethics of priority setting?

artículo científico publicado en 2006

Ethics review of big data research: What should stay and what should be reformed?

artículo científico publicado en 2021

Experimental Philosophical Bioethics

artículo científico publicado en 2020

Expertise, Ethics Expertise, and Clinical Ethics Consultation: Achieving Terminological Clarity.

artículo científico publicado en 2016

Exploring the ethics of global health research priority-setting

article

Gene editing of human embryos and designing descendants

artículo científico publicado en 2016

Healthcare professionals' understanding of the legislation governing research involving adults lacking mental capacity in England and Wales: a national survey. ⬇️

artículo científico publicado en 2018

In defence of governance: ethics review and social research.

artículo científico publicado en 2017

Is gene therapy for the treatment of male infertility ethical?

artículo científico publicado en 2008

It's unethical for general practitioners to be commissioners ⬇️

artículo científico publicado el 9 de marzo de 2011

Just Wars and doctors' strikes

scientific article published on 01 November 2016

Measuring the impact of participatory research in psychiatry: How the search for epistemic justifications obscures ethical considerations

scientific article published on 18 December 2019

Minimal Risk Remains an Open Question

journal article; published in The American Journal of Bioethics in 2011

National Standards for Public Involvement in Research: missing the forest for the trees

artículo científico publicado en 2018

New European Union regulation of clinical trials is not conflicting on deferred consent in emergency situations

scientific article published on 26 February 2013

No sex please, we're social scientists?

artículo científico publicado en 2010

On the nature and sociology of bioethics.

artículo científico publicado en 2013

Orphan drugs and the NHS: fairness in health care entails more than cost effectiveness.

artículo científico publicado en 2005

Patient and public involvement: Two sides of the same coin or different coins altogether?

artículo científico publicado en 2019

Placebo use in vaccine trials: recommendations of a WHO expert panel

artículo científico publicado en 2014

Position statement on ethics, equipoise and research on charged particle radiation therapy

artículo científico publicado en 2013

Protection by exclusion? The (lack of) inclusion of adults who lack capacity to consent to research in clinical trials in the UK

artículo científico publicado en 2019

Public involvement in the governance of population-level biomedical research: unresolved questions and future directions

artículo científico publicado en 2020

Randomization should be disclosed to potential research subjects.

artículo científico publicado en 2013

Reasonable disagreement and the justification of pre-emptive ethics governance in social research: a response to Hammersley

scientific article published on 26 June 2018

Reining in patient and individual choice.

artículo científico publicado en 2014

Research involving adults lacking capacity to consent: a content analysis of participant information sheets for consultees and legal representatives in England and Wales

article

Research led by participants: a new social contract for a new kind of research

artículo científico publicado en 2015

Should research ethics committees meet in public?

article

Standards of practice in empirical bioethics research: towards a consensus

scholarly article by Jonathan Ives et al published 10 July 2018 in BMC Medical Ethics

Structural Transformation to Attain Responsible BIOSciences (STARBIOS2): Protocol for a Horizon 2020 Funded European Multicenter Project to Promote Responsible Research and Innovation

article

The Ashley Treatment: best interests, convenience, and parental decision-making.

artículo científico publicado en 2007

The duty to disclose adverse clinical trial results.

artículo científico publicado en 2009

The new Health Research Authority framework: still work to do to facilitate high-quality public health research in English local authorities.

artículo científico publicado en 2017

The right to know and genetic testing.

artículo científico publicado en 2015

The role of emotion in ethics and bioethics: dealing with repugnance and disgust

artículo científico publicado en 2016

Toward methodological innovation in empirical ethics research

artículo científico publicado en 2012

Tragic choices in intensive care during the COVID-19 pandemic: on fairness, consistency and community

artículo científico publicado en 2020

Trust, trustworthiness and sharing patient data for research

scientific article published on 18 May 2020

Understanding and using patient experiences as evidence in healthcare priority setting

artículo científico publicado en 2019

When should patients be held responsible for their lifestyle choices?

artículo científico publicado en 2006

Lista de obras de Mark Sheehan

'It's a tough decision': a qualitative study of proxy decision-making for research involving adults who lack capacity to consent in UK

'There's more to life than money and health': Family caregivers' views on the role of Power of Attorney in proxy decisions about research participation for people living with dementia

'Your country needs you': the ethics of allocating staff to high-risk clinical roles in the management of patients with COVID-19

Assent is not consent.

Authority and the Future of Consent in Population-Level Biomedical Research

Broad consent is informed consent

Can Broad Consent be Informed Consent?

Commissioning ethically and legally: the more things change, the more they stay the same.

Constructing authentic decisions: proxy decision making for research involving adults who lack capacity to consent

Delia Smith and the ethics committee.

Developing a new justification for assent

Disclosing clinical trial results: publicity, significance and independence

Do we need research ethics committees?

Emergency medicine research: rites, rituals and consent.

Ethical review and ethical behaviour.

Ethical understandings of proxy decision making for research involving adults lacking capacity: A systematic review (framework synthesis) of empirical research

Ethics and opportunity costs: have NICE grasped the ethics of priority setting?

Ethics review of big data research: What should stay and what should be reformed?

Experimental Philosophical Bioethics

Expertise, Ethics Expertise, and Clinical Ethics Consultation: Achieving Terminological Clarity.

Exploring the ethics of global health research priority-setting

Gene editing of human embryos and designing descendants

Healthcare professionals' understanding of the legislation governing research involving adults lacking mental capacity in England and Wales: a national survey. ⬇️

In defence of governance: ethics review and social research.

Is gene therapy for the treatment of male infertility ethical?

It's unethical for general practitioners to be commissioners ⬇️

Just Wars and doctors' strikes

Measuring the impact of participatory research in psychiatry: How the search for epistemic justifications obscures ethical considerations

Minimal Risk Remains an Open Question

National Standards for Public Involvement in Research: missing the forest for the trees

New European Union regulation of clinical trials is not conflicting on deferred consent in emergency situations

No sex please, we're social scientists?

On the nature and sociology of bioethics.

Orphan drugs and the NHS: fairness in health care entails more than cost effectiveness.

Patient and public involvement: Two sides of the same coin or different coins altogether?

Placebo use in vaccine trials: recommendations of a WHO expert panel

Position statement on ethics, equipoise and research on charged particle radiation therapy

Protection by exclusion? The (lack of) inclusion of adults who lack capacity to consent to research in clinical trials in the UK

Public involvement in the governance of population-level biomedical research: unresolved questions and future directions

Randomization should be disclosed to potential research subjects.

Reasonable disagreement and the justification of pre-emptive ethics governance in social research: a response to Hammersley

Reining in patient and individual choice.

Research involving adults lacking capacity to consent: a content analysis of participant information sheets for consultees and legal representatives in England and Wales

Research led by participants: a new social contract for a new kind of research

Should research ethics committees meet in public?

Standards of practice in empirical bioethics research: towards a consensus

Structural Transformation to Attain Responsible BIOSciences (STARBIOS2): Protocol for a Horizon 2020 Funded European Multicenter Project to Promote Responsible Research and Innovation

The Ashley Treatment: best interests, convenience, and parental decision-making.

The duty to disclose adverse clinical trial results.

The new Health Research Authority framework: still work to do to facilitate high-quality public health research in English local authorities.

The right to know and genetic testing.

The role of emotion in ethics and bioethics: dealing with repugnance and disgust

Toward methodological innovation in empirical ethics research

Tragic choices in intensive care during the COVID-19 pandemic: on fairness, consistency and community

Trust, trustworthiness and sharing patient data for research

Understanding and using patient experiences as evidence in healthcare priority setting

When should patients be held responsible for their lifestyle choices?