Research misconduct gcp - Study guides, Class notes & Summaries

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Research Misconduct (GCP) Practice Exam Questions.
  • Research Misconduct (GCP) Practice Exam Questions.

  • Exam (elaborations) • 6 pages • 2024
  • Research Misconduct (GCP) Practice Exam Questions. C. Using another person's ideas, processes, results, or words without giving credit. Choose the definition for Plagiarism: A. Making up data or results and recording or reporting them. B. Changing the research record so that it does not accurately reflect the research findings. C. Using another person's ideas, processes, results, or words without giving credit. C. A and B. An informant is considered: A. a whistleblower. ...
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GCP Research Misconduct Exam Study Guide .
  • GCP Research Misconduct Exam Study Guide .

  • Exam (elaborations) • 4 pages • 2024
  • GCP Research Misconduct Exam Study Guide . The term fraud describes: a) Illegal and deceptive practices b) Fabrication c) Falsification d) plagiarism e) none of the above - CORRECT ANSWER a) Illegal and deceptive practices Regarding response to allegations of research misconduct, which of the following is CORRECT: A) The accused researcher is entitled to know who the informant is. B) The informant privacy must be protected to the extent possible and may remain anonymous c) Th...
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Research Misconduct (GCP) Questions and Answers 100% Correct
  • Research Misconduct (GCP) Questions and Answers 100% Correct

  • Exam (elaborations) • 4 pages • 2024
  • Research Misconduct (GCP)
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Research Misconduct (GCP) Questions and Answers 2024
  • Research Misconduct (GCP) Questions and Answers 2024

  • Exam (elaborations) • 4 pages • 2024
  • Research Misconduct (GCP)
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GCP TRAINING EXAM QUESTIONS CORRECTLY ANSWERED.
  • GCP TRAINING EXAM QUESTIONS CORRECTLY ANSWERED.

  • Exam (elaborations) • 26 pages • 2024
  • GCP TRAINING EXAM QUESTIONS CORRECTLY ANSWERED. After the IRB reviews and approves your protocol, informed consent, and associated documents, you should receive: A. A phone call telling you the study can now proceed. B. A personal visit from the IRB chair telling you how excited he/she is about your research. C. Written notification of the IRB decision and the approved versions of the protocol and informed consent forms. D. Nothing. If you do not receive a response in 30 days, you can...
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Social Behavioral Research Training (CITI) questions with 100% correct answers rated A+ 2023/2024
  • Social Behavioral Research Training (CITI) questions with 100% correct answers rated A+ 2023/2024

  • Exam (elaborations) • 10 pages • 2023
  • Social Behavioral Research Training (CITI) Good Clinical Practice (GCP) - correct answer international ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects Clinical Trial (NIH Def) - correct answer Beyond just biomedical studies, Social and Behavioral interventions are now defined as clinical trials. Why implement GCP? - correct answer - Protect participants - Prevent non-compliance issues - Y...
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NIH IPPCR - 2024-2025 Exam Practice Questions and Answers (100% Pass)
  • NIH IPPCR - 2024-2025 Exam Practice Questions and Answers (100% Pass)

  • Exam (elaborations) • 15 pages • 2024
  • NIH IPPCR - Exam Practice Questions and Answers (100% Pass) What describes a properly designed Case Report Form (CRF) - ️️ Collects relevant data in accordance with the protocol Allows for efficient data in accordance with the protocol Facilitates the pooling of data across studies **All of the above Scientific misconduct can cause which of the following? - ️️ Make other scientists upset because they have spent time and resources to replicate manipulated data Damage to institut...
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NIH IPPCR – 2023 Updated
  • NIH IPPCR – 2023 Updated

  • Exam (elaborations) • 9 pages • 2023
  • NIH IPPCR – 2023 UpdatedWhat describes a properly designed Case Report Form (CRF) - ANSWER Collects relevant data in accordance with the protocol Allows for efficient data in accordance with the protocol Facilitates the pooling of data across studies **All of the above Scientific misconduct can cause which of the following? - ANSWER Make other scientists upset because they have spent time and resources to replicate manipulated data Damage to institutional reputations Undermine pu...
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NIH IPPCR Exam Questions With Correct Answers
  • NIH IPPCR Exam Questions With Correct Answers

  • Exam (elaborations) • 12 pages • 2024
  • NIH IPPCR Exam Questions With Correct Answers What describes a properly designed Case Report Form (CRF) - answerCollects relevant data in accordance with the protocol Allows for efficient data in accordance with the protocol Facilitates the pooling of data across studies **All of the above Scientific misconduct can cause which of the following? - answerMake other scientists upset because they have spent time and resources to replicate manipulated data Damage to institutional reputations...
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CITI - GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus)
  • CITI - GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus)

  • Exam (elaborations) • 8 pages • 2023
  • Which of the following lists the three principles included in the Belmont Report? Respect for Persons, Beneficence, Justice Which of the following is an example of how the Principle of Beneficence can be applied to a study employing human subjects? Determining that the study has maximized benefits and minimized risks. Which of the following best describes the principle of informed consent as described in the Belmont Report? Information, comprehension, voluntariness. Module 2 ....
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