SoCRA Quizzes & Trivia

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Each and every Socra quiz that we have is made up of well-researched and interesting quiz questions. With detailed instant feedback for quiz answers, you can easily learn something new about Socra with every question you attempt.

In order to understand a disease and the effect of a certain group of medicines have on it, there have to be some clinical trials ran and SOCRA is put in place to protect the welfare of research participants. This is a review of...

Questions: 15  |  Attempts: 4854   |  Last updated: Feb 15, 2019
  • Sample Question
    What is FDA form 1571?

Exam re: forms 1571, 1572, 3454, 3455, 3500, and 3500s

Questions: 7  |  Attempts: 1955   |  Last updated: Nov 1, 2017
  • Sample Question
    Which of the following is a certification of financial interest form?

This is a review of the code of federal regulations- protecting human subjects.  Just to help with reviewing for the SOCRA exam.

Questions: 15  |  Attempts: 174   |  Last updated: Nov 1, 2017
  • Sample Question
    What is FDA form 1571?

Questions: 82  |  Attempts: 11   |  Last updated: Aug 18, 2016
  • Sample Question
    Which of the following is IRB Functions and Regulations?

Questions: 62  |  Attempts: 10   |  Last updated: Sep 21, 2017
  • Sample Question
    What are the three fundamental ethical principals for human subjects research?

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SoCRA Questions & Answers

Is it true when a short form is used for Informed Consent, the patient signs the short form ONLY and the receives a copy of both the summary and the short form?...
§ 50.27 Documentation of informed consent.(2) A short form written consent document stating that the elements of informed consent requiredby § 50.25 have been presented orally to the subject or the subject’s legally authorizedrepresen
What is 21CFR56.109 Subpart C?
56.108 IRB functions and operations. 109 is Review of Research
Which of the following are considered BASIC elements of informed consent under section 21CFR50.25 Subpart B?
1. A statement that the study involves research, an explanation of the purposes of the research and the expected duration of the subject s participation, a description of the procedures to be followed, and identification of any procedures which are e
What is 21CFR50 Subpart B?
Subpart B—Informed Consent of Human Subjects I the real true answer