Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 18:57)Exploitation | ||
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Ответ: taking unfair advantage of someone else. | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 18:57)Expression of concern | ||
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Ответ: 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. | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 18:58)Fabrication | ||
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Ответ: making up data or results | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 18:58)Falsification | ||
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Ответ: changing, omitting, or manipulating data or results deceptively; or deceptive manipulation of research materials or experiments. | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 18:59)Food and Drug Administration (FDA) | ||
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Ответ: 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. | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 19:15)Fraud | ||
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Ответ: 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. | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 19:17)Freedom of Information Act (FOIA) | ||
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Ответ: 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. | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 19:17)Good clinical practices (GCPs) | ||
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Ответ: | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 19:18)Good laboratory practices (GLPs) | ||
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Ответ: rules and procedures for designing and performing experiments or tests and recording and analyzing data rigorously. Some types of research are required by law to adhere to GLPs. | ||
Вопрос: (Последнее редактирование: пятница, 31 Июль 2020, 19:18)Good manufacturing practices (GMPs) | ||
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Ответ: rules and procedures for manufacturing a product (such as a drug) according to standards of quality and consistency. | ||