Irb practice test - Study guides, Class notes & Summaries
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ACRP Practice Exam 2022 Questions and Answers
- Exam (elaborations) • 9 pages • 2022
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[COMPANY NAME] [Company address] 
ACRP PRACTICE EXAM 
2022 QUESTIONS AND 
ANSWERS 
A subject is issued 120 tablets and is instructed to take 2 tablets 4 times a day. He 
returns 88 tablets on the morning of day 9 fasting for laboratory tests. What percent 
compliant is he? - ANSWER 50% 
To be eligible for a trial, the subjects must have liver function tests no greater than two 
times the upper limit normal and rental function tests no greater than three times the 
upper limit normal. All of t...
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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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SOCRA Practice Test Questions And Answers 2022
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Which of the following is a disclosure of financial interests form? 
FDA Form 3455 
 
 
 
Which of the following is a certification of financial interest form? 
FDA Form 3454 
 
 
 
If the investigator did have financial arrangement with the sponsor, he/she would submit the following form: 
FDA Form 3455 
 
 
 
This form is submitted by sponsor to the FDA prior to the beginning of the drug trial 
Investigational New Drug Application (1571) 
 
 
 
In the top right corner, form have OMB number. Wh...
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SOCRA - CCRP (high level) Questions and Answers (100% Correct Solutions)
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Nuremberg Code (1947) 
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 
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 if needed 
 ...
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RAC Practice Exam Questions and Answers Rated A+
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RAC Practice Exam Questions and Answers Rated A+ 
A physician reports to a manufacturer that a patient was hospitalized with acute sepsis after treatment with an approved device. This side effect is not listed in the package insert. This event must be reported by the manufacturer to FDA no later than: 
A. 5 calendar days. 
B. 15 calendar days. 
C. 30 calendar days. D. The next quarterly or annual report. C. 30 calendar days. 
Serious injury must be reported within 30 days. 21 CFR 803.50(a). 
Und...
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SOCRA Practice Test with 100% Correct Solutions
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SOCRA Practice Test with 100% Correct Solutions 
Which of the following is a disclosure of financial interests form? -Answer-FDA Form 
3455 
Which of the following is a certification of financial interest form? -Answer-FDA Form 
3454 
If the investigator did have financial arrangement with the sponsor, he/she would submit 
the following form: -Answer-FDA Form 3455 
This form is submitted by sponsor to the FDA prior to the beginning of the drug trial - 
Answer-Investigational New Drug Application...
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MEGA SOCRA CCRP EXAM CONTENT REVIEW PRACTICE TEST.
- Exam (elaborations) • 136 pages • 2024
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MEGA SOCRA CCRP EXAM CONTENT REVIEW PRACTICE TEST. 
5 - correct answer The minimum number of IRB members 
 
Subjects cannot be enrolled until IRB/IEC approval has been obtained - correct answer In a non-emergency situation, under which of the following conditions, if any, may subjects be enrolled into a study prior to IRB/IEC approval? 
 
The Sponsor - correct answer The responsibility for ensuring that the investigator understands a clinical trial lies with: 
 
A subject has been enrolled on a ...
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2024 RAC Practice Exam | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+
- Exam (elaborations) • 82 pages • 2024
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2024 RAC Practice Exam | Questions with 100% Correct Answers | Verified | Latest Update 2024| Graded A+ 
A physician reports to a manufacturer that a patient was hospitalized with acute sepsis after treatment with an approved device. This side effect is not listed in the package insert. This event must be reported by the manufacturer to FDA no later than: 
A. 5 calendar days. 
B. 15 calendar days. 
C. 30 calendar days. 
D. The next quarterly or annual report. - C. 30 calendar days. 
Serious inju...
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Test Bank for Doctor of Nursing Practice Essentials.A New Model for Advanced Practice Nursing 4th Edition Zaccagnini
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The Doctor of Nursing Practice Essentials: A New Model for Advanced Practice Nursing, 
Fourth Edition 
Mary Zaccagnini and Judith M. Pechacek 
Test Bank 
Copyright © 2020 by Jones & Bartlett Learning, LLC, an Ascend Learning Company 
Chapter 1: Nursing Science and Theory: Scientific Underpinnings for Practice 
Multiple Choice 
1. Which metaparadigm concept is generally accepted as part of the body of knowledge in 
nursing? 
a. Illness 
b. Environment 
c. Chronicity 
d. Patient 
Answer: b 
2. Wh...
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ULL NURSING 104 FINAL EXAM QUESTIONS & ANSWERS, SOLVED 100% CORRECT!!
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State Board's process if you did something bad. - they first investigate, then they put you into a 
program to help with whatever you did, they are never looking to take your license (as long as what you 
did was not to intentionally to harm someone else) 
Affordable Care Act - An expansion of medicaid, most of employers must provide health 
insurance, have insurance or face surtax, prevents rejection based on pre-existing condition. Also 
referred to as "Obamacare", signed into law in 2010. ...
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