Question: (Last edited: Friday, 31 July 2020, 7:17 PM)Freedom of Information Act (FOIA) | ||
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Answer: a law enacted in the U.S. and other countries which allows the public to obtain access to government documents, including documents related to government-funded scientific research, such as data, protocols, and emails. Several types of documents are exempt from FOIA requests, including classified research and confidential information pertaining to human subjects research. | ||
Question: (Last edited: Friday, 31 July 2020, 7:15 PM)Fraud | ||
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Answer: knowingly misrepresenting the truth or concealing a material (or relevant) fact to induce someone to make a decision to his or her detriment. Some forms of research misconduct may also qualify as fraud. A person who commits fraud may face civil or criminal legal liability. | ||
Question: (Last edited: Friday, 31 July 2020, 6:59 PM)Food and Drug Administration (FDA) | ||
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Answer: a federal agency in charge of approving the marketing of drugs, biologics, medical devices, cosmetics, and food additives. The FDA has adopted human subjects research regulations which are similar to the Common Rule; however, the FDA rules do not allow exceptions from informed consent requirements unless a study qualifies as Emergency research. | ||
Question: (Last edited: Friday, 31 July 2020, 6:58 PM)Falsification | ||
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Answer: changing, omitting, or manipulating data or results deceptively; or deceptive manipulation of research materials or experiments. | ||
Question: (Last edited: Friday, 31 July 2020, 6:58 PM)Fabrication | ||
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Answer: making up data or results | ||
Question: (Last edited: Friday, 31 July 2020, 6:57 PM)Expression of concern | ||
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Answer: a journal may publish an expression of concern when a paper has come under suspicion for wrongdoing or is being investigated for possible research misconduct. | ||
Question: (Last edited: Friday, 31 July 2020, 6:57 PM)Exploitation | ||
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Answer: taking unfair advantage of someone else. | ||
Question: (Last edited: Friday, 31 July 2020, 6:56 PM)Expedited review | ||
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Answer: in human subjects research, review of a study by the chair of an institutional review board (or designee) instead of by the full board. Expedited review may be conducted on new studies that pose minimal risks to subjects, for continuing review in which a study is no longer recruiting subjects, or on amendments to approved studies that make only minor changes. | ||
Question: (Last edited: Friday, 31 July 2020, 6:56 PM)Exculpatory language | ||
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Answer: language in an informed consent form, contract, or other document intended to excuse a party from legal liability. | ||
Question: (Last edited: Friday, 31 July 2020, 6:55 PM)Exempt research | ||
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Answer: human subjects research which is exempted from review by an institutional review board. Some types of exempt research include research on existing human samples or data in which the researcher cannot readily identify individuals and anonymous surveys of individuals. | ||