No abstract available
MeSH terms
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Consent Forms
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Cost-Benefit Analysis
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Drug-Related Side Effects and Adverse Reactions*
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Drugs, Investigational*
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Ethical Review*
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Ethics Committees*
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Ethics Committees, Research*
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Ethics*
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Federal Government
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Government
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Government Regulation
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Human Experimentation*
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Humans
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Informed Consent
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Mandatory Reporting
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Research Personnel
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Research Subjects
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Risk
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Risk Assessment
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Social Control, Formal
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United States
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United States Food and Drug Administration