Glossary
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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, 6:58 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, 6:59 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, 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, 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. | |||