Public participation in medical research and biobanking is considered key to advances in
scientific discovery and translation to improved health care. Cultural concerns relating to …

As part of a (bio) colonial project, the biological information of Indigenous Peoples has
historically been under scientific scrutiny, with very limited benefits for communities and …

Background Researchers are required to seek consent from Indigenous communities prior
to conducting research but there is inadequate information about how Indigenous people …

Thousands of blood samples taken from Australia's indigenous people lie in institutional
freezers of the global North, the legacy of a half-century of scientific research. Since those …

Recent ethics guidelines and policies are changing the way health research is understood,
governed, and practiced among Aboriginal communities in Canada. This provides a unique …

Objectives The second edition (2010) of the Tri-Council Policy Statement on Ethical Conduct
for Research Involving Humans (TCPS2) prescribes a set of principles and provisions for …

Blood samples collected from members of indigenous communities in the mid‐20th century
by scientists interested in human variation remain frozen today in institutional repositories …

While human genetic research promises to deliver a range of health benefits to the
population, genetic research that takes place in Indigenous communities has proven …

The ethics of research involving Aboriginal populations and low and middle-income country
populations each developed out of a long history of exploitative research projects and …

This article is based on ethnographic fieldwork conducted with the Indian community in
Houston, as part of a NIH–NHGRI‐sponsored ethics study and sample collection initiative …