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    • Topic life green Beginning of life
      • Donor conception
      • Disagreements in the care of critically ill children
      • Egg freezing
      • Genome editing and human reproduction
      • Mitochondrial DNA disorders
      • Neonatal medicine and care
      • Non-invasive prenatal testing
      • Whole genome sequencing of babies
    • Topic health green Health and society
      • COVID-19
      • Ageing
      • Cosmetic procedures
      • Dementia
      • Donation of bodily material
      • Experimental treatments
      • Gender identity
      • Genetics and genomics
      • Medical implants
      • Mental disorders
      • Naturalness
      • Personalised healthcare
      • Public health
      • Screening
      • Solidarity
      • Vaccination
    • Topic environment green Animals, food and environment
      • Animal research
      • Biofuels
      • Genome editing and farmed animals
      • GM crops
      • Meat alternatives
      • Xenotransplantation
    • Topic research green Research ethics
      • Children and clinical research
      • Culture of scientific research
      • Embryo and stem cell research
      • Research in developing countries
      • Research in global health emergencies
    • Topic technology green Data and technology
      • AI in healthcare and research
      • Biological and health data
      • Emerging biotechnologies
      • Forensic use of bioinformation
      • Neurotechnology
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Policy

The Council engages with parliamentarians and others to inform policy and promote debate about bioethics issues.

Consultation Response

01 Aug 2015

The Right to Know - Response to Discussion Paper

Government of Victoria, Australia

Tagged: Donor conception

Consultation Response

01 Jul 2015

Comments on WMA draft Declaration on Ethical Considerations regarding Health Databases and Biobanks

World Medical Association

Tagged: biodata

Policy Briefing Paper

01 Jul 2015

Ethical challenges in bioscience and health policy for the new UK Parliament

Consultation Response

01 Jul 2015

HFEA consultation: Regulating mitochondrial donation

Human Fertilisation and Embryology Authority (HFEA)

Tagged: Mitochondrial DNA disorders

Consultation Response

01 Jul 2015

Response to the Committee’s Call for Evidence on the impact on people with disabilities of the Equality Act 2010

House of Lords Select Committee on the Equality Act 2010 and Disability

Consultation Response

01 Jun 2015

Response to the Global Alliance for Genomics & Health Consent Policy

Global Alliance for Genomics & Health

Tagged: biodata

Consultation Response

01 May 2015

Response to UK policy framework for health and social care research: call for comments

Health Research Authority (HRA)

Tagged: children and clinical research

Policy Briefing Paper

01 May 2015

Key recommendations in the Council's report - Children and clinical research: ethical issues

Tagged: children and clinical research

Consultation Response

01 Apr 2015

Response to Nurse Review of Research Councils: Call for Evidence

Department for Business, Innovation & Skills

Tagged: biodata

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About us

The Nuffield Council on Bioethics is an independent body that examines and reports on ethical issues in biology and medicine. It was established by the Trustees of the Nuffield Foundation in 1991, and since 1994 it has been funded jointly by the Foundation, Wellcome and the Medical Research Council.

Find out more
News
  • 20 Apr 2021
    Trust is a key factor in vaccine uptake, says new briefing by ethics body
    Read post
  • 15 Apr 2021
    New UK pandemic ethics accelerator
    Read post

Nuffield Council on Bioethics 28 Bedford Square London, WC1B 3JS

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+44 (0)20 7681 9619

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bioethics@nuffieldbioethics.org

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