Human subject protections - Study guides, Class notes & Summaries

The Federal Regulations – SBE Questions and Answers Graded A+ Who enforces the Common Rule? The Office for Human Research Protections (OHRP) enforces the Common Rule in federally funded research. What is the definition of "human subject" under federal regulations? A human subject is a living individual about whom a researcher obtains data through intervention or interaction or gathers identifiable private information. What is a research protocol? A research protocol is a doc...

CITI Federal Regulations SBE Questions and Answers Rated A+ What is the purpose of the Common Rule in human subjects research? The Common Rule provides ethical guidelines and regulations to ensure the protection of human subjects involved in research. When is it necessary to obtain informed consent from research participants? Informed consent must be obtained before any participant engages in research to ensure they understand the purpose, risks, and benefits. What is the role of...

CITI Training Exam Questions and Answers 100% Correct Three principles of Belmont Report - Correct Answer ️️ -Respect for Persons Beneficence Justice The Belmont Report Principle of Beneficence - Correct Answer ️️ -MAXIMIZATION of benefits and MINIMIZATION of risks T/F Belmont Report indicates it is necessary to rigorously avoid conflicts of interest - Correct Answer ️️ -TRUE The Belmont Report Respect for Person - Correct Answer ️️ -Requires that subjects freely choos...

CITI History and Ethical Principles – SBE Latest Update Graded A+ What historical event significantly changed the landscape of research ethics? The Tuskegee Syphilis Study revealed the need for ethical standards in research involving human subjects. What does "respect for persons" entail in research ethics? It involves acknowledging autonomy and obtaining informed consent from participants. How does beneficence relate to research practices? Beneficence means maximizing benefi...

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...

Informed Consent correct answersA statement that the study involves research. Explanation of purpose of research. Expected duration of subject's participation. Procedures to be followed. Identification of experimental procedures. Reasonably foreseeable risks or discomforts. Benefits to subject or to others expected. Statement describing confidentiality of records identifying the subject. Disclosure of alternative procedures and treatment. Explanation of Compensation for Injury. Who to contact w...

Informed Consent -Answer A statement that the study involves research. Explanation of purpose of research. Expected duration of subject's participation. Procedures to be followed. Identification of experimental procedures. Reasonably foreseeable risks or discomforts. Benefits to subject or to others expected. Statement describing confidentiality of records identifying the subject. Disclosure of alternative procedures and treatment. Explanation of Compensation for Injury. Who to contact with...

You are the security subject matter expert (SME) for an organization considering a transition from the legacy environment into a hosted cloud provider 's data center. One of the challenges you 're facing is whether the cloud provider will be able to comply with the existing legislative and contractual frameworks your organization is required to follow. This is a _________ issue. a. Resiliency b. Privacy c. Performance d. Regulatory D 76. You are the security subject matter expert (SME) ...

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...

CIPP/E Questions and Answers Already Graded A Universal Declaration of Human Rights (UDHR) 1948, Art. 12 i. First international legal instrument announcing a right to privacy ii. Catalyst for other human rights instruments in Europe. iii. Recognized universal values and traditions of "the inherent dignity and the equal and inalienable rights of all members of the human race in the foundation of freedom, justice, and peace in the world." European Convention on Human Rights (ECHR) 1950, Art. 8 ...