Nuremberg trial - Study guides, Class notes & Summaries
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SOCRA - CCRP (high level) Exam Questions & Answers 2023/2024
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SOCRA - CCRP (high level) Exam Questions & Answers 2023/2024 
 
 
Nuremberg Code (1947) - ANSWER-A research ethics code that arose in response to the Nazis' inhumane experimentation (nuremberg trials) - holocaust, racial hygiene / eugenics / master race. 
 
The Nuremberg Code - 10 points - ANSWER-1. voluntary 
2. necessary for results 
3. logical design and results 
4. avoid unnecessary harm 
5. cannot result in death or disablement 
6. risk assessment 
7. protect subjects against harm 
8. qual...
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SOCRA - CCRP (high level) Questions & Answers(RATED A+)
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Nuremberg Code (1947) - ANSWERA research ethics code that arose in response to the Nazis' inhumane experimentation (nuremberg trials) - holocaust, racial hygiene / eugenics / master race. 
 
The Nuremberg Code - 10 points - ANSWER1. voluntary 
2. necessary for results 
3. logical design and results 
4. avoid unnecessary harm 
5. cannot result in death or disablement 
6. risk assessment 
7. protect subjects against harm 
8. qualified investigators 
9. right to withdrawal 
10. right to end tria...
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SOCRA - CCRP FDA and HHS Regulations and Disclosures Practice Exam Questions and Answers 2023/2024
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SOCRA - CCRP FDA and HHS Regulations and Disclosures Practice Exam Questions and Answers 2023/2024 
Nuremberg Code (1947) - correct answer A research ethics code that arose in response to the Nazis' inhumane experimentation (nuremberg trials) - holocaust, racial hygiene / eugenics / master race. 
 
The Nuremberg Code - 10 points - correct answer 1. voluntary 
2. necessary for results 
3. logical design and results 
4. avoid unnecessary harm 
5. cannot result in death or disablement 
6. risk ass...
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IRB Review Questions Correctly Answered.
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IRB Review Questions Correctly Answered. 
 
A subject in a clinical research trial experiences a serious, unanticipated adverse drug experience. How should the investigator proceed, with respect to the IRB, after the discovery of the adverse event occurrence? - CORRECT ANSWER Report the adverse drug experience in a timely manner, in keeping with the IRB's policies and procedures, using the forms or the mechanism provided by the IRB. 
 
The most appropriate action for the investigator to take...
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SOCRA - CCRP (high level) exam 2024 with 100% complete solutions
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Nuremberg Code (1947) correct answersA research ethics code that arose in response to the Nazis' inhumane experimentation (nuremberg trials) - holocaust, racial hygiene / eugenics / master race. 
 
The Nuremberg Code - 10 points correct answers1. voluntary 
2. necessary for results 
3. logical design and results 
4. avoid unnecessary harm 
5. cannot result in death or disablement 
6. risk assessment 
7. protect subjects against harm 
8. qualified investigators 
9. right to withdrawal 
10. right...
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ACRP- Clinical Research Knowledge Assessment (CRKA)
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ACRP- Clinical Research Knowledge Assessment (CRKA) 
True or false? Direct communication between a sponsor and IRB/IEC is expressly prohibited per GCP. - Correct Answers False 
 
As part of their risk assessment process the sponsor determines that there is a high likelihood that enrollment in the trial will be challenging and slow. Which of the following is the best choice in this situation: 
a. The sponsor should develop a risk management plan to handle this operational risk 
b. The sponsor sho...
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2023 CCRP Exam Prep| 30 PAGES(300 QUESTIONS)| WITH COMPLETE SOLUTIONS
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2023 CCRP Exam Prep| 30 PAGES(300 
QUESTIONS)| WITH COMPLETE SOLUTIONS 
Who was tried in the Nuremburg Military Tribunals and why? Correct Answer: Doctors who 
committed war crimes against humanity including medical experiments on concentration camp 
inmates and other human subjects without consent 
What was the outcome of the Nuremburg Military Tribunals? Correct Answer: After 140 days 
of proceedings with testimony of 85 witnesses and submission of 1,500 documents, American 
judges convicted 1...
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SOCRA Test practice Questions and Answers 2024
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SOCRA Test practice Questions and Answers 2024 
The Purpose of the IRB is to: -Answer-Protect the rights and welfare of human subjects 
in research 
What is the minimum number of members required by an IRB -Answer-5 
Which of the following are necessary to waive consent? 
A.Subject is unable to give consent 
B.No time or unable to contact next of kin 
C.Life-Threatening Condition 
D.No other treatment available 
E.All of the above -Answer-all of the above 
This form is used for the mandatory rep...
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CCRP Exam Prep Exam Questions with Correct Solutions| Rated A+
- Exam (elaborations) • 37 pages • 2023
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Who was tried in the Nuremburg Military Tribunals and why? - Doctors who committed war crimes against humanity including medical experiments on concentration camp inmates and other human subjects without consent 
 
What was the outcome of the Nuremburg Military Tribunals? - After 140 days of proceedings with testimony of 85 witnesses and submission of 1,500 documents, American judges convicted 16 doctors on 8/20/1947. Seven were sentenced to death and executed 6/2/1948. 
 
What historical ...
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CITI Training Questions and Answers
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Belmont Report and its principles - AnswerWhich of the following is an example of how the principle of beneficence can be applied to a study 
employing human subjects? - Answer-Determining that the study has a maximization of the benefits and 
a minimization of risks 
Which of the following are the three principles discussed in the Belmont Report? - Answer-respect for 
persons, beneficence, justice 
The Belmont Report's principle of respect for persons incorporates at least two ethical convicti...
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