Explain the concept of clinical equipoise

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Reference no: EM133831577

Question

1. Explain the concept of clinical equipoise and its implications for the use of placebo controls.

2. Explain why IRBs are not supposed to consider "collateral benefits" to subjects as part of the process of risk-benefit assessment.

3. Under U.S. law, in what circumstances are individuals injured as a result of participating in clinical research entitled to compensation? How did the Presidential Commission recommend changing the system?

Reference no: EM133831577

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