The nuremberg code - Study guides, Class notes & Summaries

CCRP Certification Exam Quiz with Approved Answers | Latest 2023/2024 Year/ description of the Nuremberg Code ️1947- German physicians conducted unethical experiments on concentration camp prisoners without their consent. What implications came of the Nuremberg Code? ️Ten elements of human research including voluntary informed consent is absolutely essential. Year and description of the Declaration of Helsinki ️1964- Based on the principles of the Nuremberg code. This declaration l...

Which of the following was the result of the Beecher article? - Answer- Realization that ethical abuses are not limited to the Nazi regime Issued in 1974, 45 CFR 46 raised to regulatory status: - Answer- US Public Health Service Policy The use of prisoners in research is a concern under the Belmont principle of Justice because: - Answer- Prisoners may not be used to conduct research that only benefits the larger society Which of the following is included in the Nuremberg Code: - Answer-...

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 docume...

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. qualified investigators 9. right to withdrawal 10. right to end trial ...

CITI -Social Behavioral Research Questions and Answers What procedures must be described in an agreement called an "assurance of compliance" with OHRP? Procedures in place that ensure that subjects will be protected in a manner commensurate with the Common Rule, including review by an independent committee comparable to an IRB. A researcher proposes to conduct a study at a foreign site that has been determined to be exempt from the federal regulations by institutional policy. Accordi...

CITI Social-Behavioral-Educational Researchers Questions and Answers Graded A+ Belmont Report provides the ethical framework for the federal regulations designed to protect human research subjects. Belmont Report and Its Principles The Belmont Report's principle of respect for persons incorporates at least two ethical convictions: first, that individuals should be treated as autonomous agents, and second, that: Persons with diminished autonomy are entitled to protection. ...

CCRP Exam 2024 with 100%Correct Answers. How many days does a sponsor have to report an emergency use of an IP to the FDA? correct answer5 working days How many members must sit on an IRB? correct answer5 How long must an IRB retain records per 21 CFR 56? correct answer3 years after completion of research What are the criteria for IRB approval of research? (7) correct answer1. Risks to subjects are minimized 2. Risks are reasonable in relation to anticipated benefits 3. Selection of subje...

Belmont Report was created as part of? Correct Answer: The national Research Act of 1974. Who was the Belmont Report formulated by? Correct Answer: The National Commission for the protection of human subjects in biomedical and behavioral research. What year was the publication of the FDA regulations made? Correct Answer: 1980 *1981 for the HHS and revised FDA Regulations. What year was GCP and HIPAA created? Correct Answer: 1996 What is the National Research Act? Correct Answer: ...

CCRP Exam 2024 with 100%Correct Answers. How many days does a sponsor have to report an emergency use of an IP to the FDA? correct answer5 working days How many members must sit on an IRB? correct answer5 How long must an IRB retain records per 21 CFR 56? correct answer3 years after completion of research What are the criteria for IRB approval of research? (7) correct answer1. Risks to subjects are minimized 2. Risks are reasonable in relation to anticipated benefits 3. Selection of subj...

SOCRA CCRP EXAM 2024 WITH 100% CORRECT ANSWERS When was the Nuremberg Code created? - correct answer 1947 What did the Nuremberg Code establish? - correct answer Worldwide requirement for informed consent with properly formulated experimentation with beneficence towards participants. When was Belmont report established? - correct answer 1979 What does the Belmont report do? - correct answer - Establish boundaries between practice and research - created ethical principles: Respect ...