Double-blinding is the assigning of subjects randomly to both experimental and control groups.
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Q18: For most clinical trials, randomization is unnecessary.
Q19: The safety and effectiveness of a treatment
Q20: There is substantial agreement in bioethics on
Q21: A typical clinical trial will consist of
Q22: The U.S. government never formally apologized for
Q24: Often, a single well-crafted clinical trial can
Q25: Before human studies can begin, a treatment
Q26: There is consensus that to be ethically
Q27: Most bioethicists agree that the use of
Q28: Women have historically been excluded as subjects
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