Biomedical research is increasingly carried out in low- and
middle-income countries. International consensus has largely been
achieved around the importance of valid consent and protecting
research participants from harm. But what are the responsibilities
of researchers and funders to share the benefits of their research
with research participants and their communities? After setting out
the legal, ethical and conceptual frameworks for benefit sharing,
this collection analyses seven historical cases to identify the
ethical and policy challenges that arise in relation to benefit
sharing. A series of recommendations address possible ways forward
to achieve justice for research participants in low- and
middle-income countries.
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