Socra exam practice Study guides, Class notes & Summaries

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SoCRA CERTIFICATION EXAM AND PRACTICE EXAM 2023-2024 ACTUAL EXAMS 400 QUESTIONS AND CORRECT DETAILED ANSWERS WITH RATIONALES (VERIFIED ANSWERS) | ALREADY GRADED A+   Popular
  • SoCRA CERTIFICATION EXAM AND PRACTICE EXAM 2023-2024 ACTUAL EXAMS 400 QUESTIONS AND CORRECT DETAILED ANSWERS WITH RATIONALES (VERIFIED ANSWERS) | ALREADY GRADED A+

  • Exam (elaborations) • 145 pages • 2023 Popular
  • SoCRA CERTIFICATION EXAM AND PRACTICE EXAM 2023-2024 ACTUAL EXAMS 400 QUESTIONS AND CORRECT DETAILED ANSWERS WITH RATIONALES (VERIFIED ANSWERS) | ALREADY GRADED A+
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CCRP SOCRA Exam - Practice Exam #1 Questions and Answers 2023
  • CCRP SOCRA Exam - Practice Exam #1 Questions and Answers 2023

  • Exam (elaborations) • 11 pages • 2023
  • CCRP SOCRA Exam - Practice Exam #1 Questions and Answers 2023 The responsibility for ensuring that the investigator understands a clinical trial lies with which individual/or organization? A) FDA B) IRB C) Sponsor D) Coordinator C) Sponsor What is the minimum number of IRB Members? A) 3 B) 5 C) 6 D) 10 B) 5 A significant risk device is defined as an investigational device that is: A) Intended as an implant and presents a potential for serious risk to the health, s...
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SOCRA EXAM PREP | 2023/ 2024 Newly Updated | ALL EXAMS COMBINED| Questions and Verified Answers| Highly Rated Guide Popular
  • SOCRA EXAM PREP | 2023/ 2024 Newly Updated | ALL EXAMS COMBINED| Questions and Verified Answers| Highly Rated Guide

  • Exam (elaborations) • 356 pages • 2023
  • SOCRA EXAM PREP | 2023 Update | Questions and Verified Answers| Highly Rated Guide Q: What 4 aspects of a trial should a sponsor focus on when monitoring for compliance per 21 CFR 312.56? Answer: 1) Progress of investigations under IND 2) Secure compliance or discontinue investigators that are not compliant and notify FDA 3) Review safety/effectiveness of drug and report safety issues to FDA + make annual reports or progress 4) Notify FDA, all IRBs and all investigators if drug presen...
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CCRP SOCRA Exam - Practice Exam with 100% Correct Answers | Latest 2023/2024
  • CCRP SOCRA Exam - Practice Exam with 100% Correct Answers | Latest 2023/2024

  • Exam (elaborations) • 12 pages • 2023
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  • CCRP SOCRA Exam - Practice Exam with 100% Correct Answers | Latest 2023/2024 The responsibility for ensuring that the investigator understands a clinical trial lies with which individual/or organization? A) FDA B) IRB C) Sponsor D) Coordinator ️ C) Sponsor What is the minimum number of IRB Members? A) 3 B) 5 C) 6 D) 10 ️ B) 5 A significant risk device is defined as an investigational device that is: A) Intended as an implant and presents a potential for serious risk to the heal...
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CCRP SOCRA Exam Practice Exam #1 With Answers 2023.
  • CCRP SOCRA Exam Practice Exam #1 With Answers 2023.

  • Exam (elaborations) • 10 pages • 2023
  • CCRP SOCRA Exam Practice Exam #1 With Answers 2023.
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CCRP SOCRA Exam Practice Exam #1 With Answers 2023.
  • CCRP SOCRA Exam Practice Exam #1 With Answers 2023.

  • Exam (elaborations) • 10 pages • 2023
  • CCRP SOCRA Exam Practice Exam #1 With Answers 2023.
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Practice Questions for SOCRA exam VERIFIED 2022/2023
  • Practice Questions for SOCRA exam VERIFIED 2022/2023

  • Exam (elaborations) • 8 pages • 2022
  • Practice Questions for SOCRA exam VERIFIED 2022/2023Which of the following is a disclosure of financial interests form? ... Which of the following is a certification of financial interest form? ... 00:27 01:29 If the investigator did have financial arrangement with the sponsor, he/she would submit the following form: ... This form is submitted by sponsor to the FDA prior to the beginning of the drug trial Investigational New Drug Application In the top rig...
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SOCRA Exam Practice Questions With VERIFIED Answers 2022/2023
  • SOCRA Exam Practice Questions With VERIFIED Answers 2022/2023

  • Exam (elaborations) • 9 pages • 2023
  • SOCRA Exam Practice Questions With VERIFIED Answers 2022/2023
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