Abstract
Informed consent in clinical research is a matter of both ethics and federal regulation. A research subject must enter a study voluntarily, be informed about risks and benefits, and understand the difference between experiment and treatment.
| Original language | English |
|---|---|
| Pages (from-to) | 907-910 |
| Number of pages | 4 |
| Journal | Cleveland Clinic Journal of Medicine |
| Volume | 71 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - Nov 2004 |
| Externally published | Yes |
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