This paper explores social relations within the 'trial community' (staff and volunteers) of a Malaria Vaccine Trial (MVT), implemented by the Medical Research Council (MRC) in The Gambia between 2001 and 2004. It situates ethical concerns with medical research within the everyday life of scientific fieldwork. Based upon discussions with volunteers and staff, we explore processes of mediation between scientific project and study population, and between formal ethics, local ethical debates and everyday practice. We observe that material contact and substantial transactions, notably of blood and medicine, are central to the construction of the MVT. These transactions are guided by a concrete and relational form of ethics, which contrasts with ...
This study explores ethical issues raised in providing medical care to participants and communities ...
Human Infection Studies (HIS) have emerged as an important research approach with the potential to f...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...
This paper describes a malaria research project in The Gambia to provoke thinking on the social valu...
AbstractThis paper describes a malaria research project in The Gambia to provoke thinking on the soc...
This paper describes a malaria research project in The Gambia to provoke thinking on the social valu...
This paper describes a malaria research project in The Gambia to provoke thinking on the social valu...
This thesis provides an in-depth look at clinical trials in low-resource settings and the effects of...
AbstractThis paper describes a malaria research project in The Gambia to provoke thinking on the soc...
Clinical trials conducted in low-resource settings have unique challenges associated with their cond...
Clinical trials conducted in low-resource settings have unique challenges associated with their cond...
Controlled human malaria infection (CHMI) studies involve the deliberate infection of healthy volunt...
Critiques of biomedical research in low-resource settings typically centre on clinical trials and th...
Community Engagement (CE) has been presented by bio-ethicists and scientists as a straightforward an...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...
This study explores ethical issues raised in providing medical care to participants and communities ...
Human Infection Studies (HIS) have emerged as an important research approach with the potential to f...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...
This paper describes a malaria research project in The Gambia to provoke thinking on the social valu...
AbstractThis paper describes a malaria research project in The Gambia to provoke thinking on the soc...
This paper describes a malaria research project in The Gambia to provoke thinking on the social valu...
This paper describes a malaria research project in The Gambia to provoke thinking on the social valu...
This thesis provides an in-depth look at clinical trials in low-resource settings and the effects of...
AbstractThis paper describes a malaria research project in The Gambia to provoke thinking on the soc...
Clinical trials conducted in low-resource settings have unique challenges associated with their cond...
Clinical trials conducted in low-resource settings have unique challenges associated with their cond...
Controlled human malaria infection (CHMI) studies involve the deliberate infection of healthy volunt...
Critiques of biomedical research in low-resource settings typically centre on clinical trials and th...
Community Engagement (CE) has been presented by bio-ethicists and scientists as a straightforward an...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...
This study explores ethical issues raised in providing medical care to participants and communities ...
Human Infection Studies (HIS) have emerged as an important research approach with the potential to f...
Individual informed consent is a key ethical obligation for clinical studies, but empirical studies ...