Regulation of biomedical research in Africa | The BMJ Skip to main content Intended for
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National advisory committees have considered the obligations owed to research participants
in the event of research-related injuries. These committees have repeatedly concluded that …

There is an emerging ethical consensus that injured research participants should receive
medical care and compensation for their research-related injuries. This consensus is …

The past several years have seen an evolution in the obfigations of pharmaceutical
companies conducting clinical trials abroad. Kejplyers, such as international human, ghts …

Concern has been voiced in the research ethics literature that under US federal regulations
US sponsors, particularly the NIH, are not required to provide compensation for the …

In view of ongoing violations of international ethical codes, and the exploitation of vulnerable
participants during biomedical research in developing countries, it would be advisable for …

Sažetak Biomedical research is important for development of science, diagnostics and
production of new, effective methods of treatment, with lowest possible risk. Biomedical …

Sažetak Biomedicinska istraživanja važna su za razvoj znanosti, dijagnostiku i proizvodnju
novih, učinkovitih metoda liječenja, sa što manje mogućeg rizika. Njihovo provođenje na …

Clinical trials constitute a critical aspect of regulatory affairs in the biomedical device
industry. Class III devices, which are defined as highly regulated, high-risk instruments that …