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The Conversation
The Conversation
Joel Lexchin, Associate professor, Department of Family and Community Medicine, University of Toronto; York University, Canada; University of Sydney

In drug trials, lack of oversight of research ethics boards could put Canadian patients at risk

Research ethics boards are supposed to ensure that, among other things, patients understand the nature of the research and have given informed consent. (Unsplash/Nappy)

New drug approvals by Health Canada are based on the results of clinical trials. But before clinical trials can go ahead, they need to be approved by ethics committees known as Research Ethics Boards (REBs).

Virtually all hospitals where research is conducted have REBs, as do universities and other institutions. The REBs are supposed to ensure that patients understand the nature of the research and have given informed consent, that the trials are conducted in an ethical way that minimizes any harm to them and that the investigators are competent to do the research.

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