Ccrp test - Study guides, Class notes & Summaries

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Socra CCRP test questions and answers
  • Socra CCRP test questions and answers

  • Exam (elaborations) • 4 pages • 2024
  • Socra CCRP test questions and answers
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ACRP CCRA EXAM PREP TEST RATED 100% CORRECT
  • ACRP CCRA EXAM PREP TEST RATED 100% CORRECT

  • Exam (elaborations) • 26 pages • 2023
  • ACRP CCRA EXAM PREP TEST RATED 100% CORRECT
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ACRP CCRC EXAM PREP TEST RATED 100% CORRECT
  • ACRP CCRC EXAM PREP TEST RATED 100% CORRECT

  • Exam (elaborations) • 30 pages • 2023
  • ACRP CCRC EXAM PREP TEST RATED 100% CORRECT
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CCRP SOCRA Exam - Practice Exam #1 (Practice Test #1 (Ethics, 21 CFR Parts 50, 56, 312, 812; 45 CFR Part 46) Past questions directly from SOCRA) Passed Qs & As
  • CCRP SOCRA Exam - Practice Exam #1 (Practice Test #1 (Ethics, 21 CFR Parts 50, 56, 312, 812; 45 CFR Part 46) Past questions directly from SOCRA) Passed Qs & As

  • Exam (elaborations) • 10 pages • 2024
  • CCRP SOCRA Exam - Practice Exam #1 (Practice Test #1 (Ethics, 21 CFR Parts 50, 56, 312, 812; 45 CFR Part 46) Past questions directly from SOCRA) Passed Qs & As
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SOCRA CCRP Test Questions with Correct Solutions | Graded A+
  • SOCRA CCRP Test Questions with Correct Solutions | Graded A+

  • Exam (elaborations) • 5 pages • 2023
  • Contract Research Organization - A person or an organization (commercial, academic, or other) contracted by the sponsor to perform one or more of a sponsor's trial-related duties and functions. When a short form is used for informed consent the witness must sign the short form or the summary? - False-they must sign both What is FDA form 3454 - Certification Financial Interests and Arrangements of Clinical Investigators What are the three main basic ethical principles of the B...
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CCRP SoCRA Exam Latest Update Rated A
  • CCRP SoCRA Exam Latest Update Rated A

  • Exam (elaborations) • 12 pages • 2024
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  • CCRP SoCRA Exam Latest Update Rated A 21 CFR Part 11 Electronic Records; Electronic Signatures 21 CFR Part 11 Subpart B Electronic Records 21 CFR Part 11 Subpart C Electronic Signatures 21 CFR Part 50 Protection of Human Subjects 21 CFR Part 50 Subpart B Informed Consent of Human Subjects 21 CFR Part 50 Subpart D Additional Safeguards for Children in Clinical Investigations 21 CFR Part 56 Institutional Review Board 21 CFR Part 56 Subpart B Organization and Personnel 21 CFR Part 56 Subpa...
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Socra CCRP Exam Prep Test 2024- with 100% Correct Answers ( A Graded
  • Socra CCRP Exam Prep Test 2024- with 100% Correct Answers ( A Graded

  • Exam (elaborations) • 7 pages • 2024
  • Socra CCRP Exam Prep Test 2024- with 100% Correct Answers ( A Graded
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CCRP ADVANCED TEST QUESTIONS AND ANSWERS RATED A+.
  • CCRP ADVANCED TEST QUESTIONS AND ANSWERS RATED A+.

  • Exam (elaborations) • 13 pages • 2024
  • CCRP ADVANCED TEST QUESTIONS AND ANSWERS RATED A+. Sponsor - correct answer An entity that initiates a clinical investigation 3 primary responsibilities of an investigator - correct answer 1. Oversees the conduct of the clinical trial 2. Protects the rights, safety, and welfare of subjects 3. Control the use of investigational product FDA Form 1572 - correct answer Statement of Investigator Form - Signed Declaration from investigator that he/she will comply with FDA regulations When sh...
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