Certified clinical r - Study guides, Class notes & Summaries

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SOCRA-Certified Clinical Research Professional (CCRP) Exam Questions Containing 199 Terms with Certified Answers 2024.
  • SOCRA-Certified Clinical Research Professional (CCRP) Exam Questions Containing 199 Terms with Certified Answers 2024.

  • Exam (elaborations) • 32 pages • 2024
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  • SOCRA-Certified Clinical Research Professional (CCRP) Exam Questions Containing 199 Terms with Certified Answers 2024.
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(219 Questions) Certified Clinical Research Associate Exam Study Guide (Latest 2024)
  • (219 Questions) Certified Clinical Research Associate Exam Study Guide (Latest 2024)

  • Exam (elaborations) • 69 pages • 2023
  • (219 Questions) Certified Clinical Research Associate Exam Study Guide (Latest 2024)
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Certified Clinical Research Professional Questions and Answers 2024
  • Certified Clinical Research Professional Questions and Answers 2024

  • Exam (elaborations) • 6 pages • 2024
  • Certified Clinical Research Professional Questions and Answers 2024
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Certified Clinical Research Professional (CCRP) Final Board Certification Questions and Answers 2023/2024
  • Certified Clinical Research Professional (CCRP) Final Board Certification Questions and Answers 2023/2024

  • Exam (elaborations) • 149 pages • 2024
  • Certified Clinical Research Professional (CCRP) Final Board Certification Questions and Answers 2023/2024 The minimum number of IRB members - correct answer 5 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 responsibility for ensuring that the investigator understands a clinical trial lies with - correct a...
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Certified Clinical Research Professional (CCRP) Exam 100% Pass
  • Certified Clinical Research Professional (CCRP) Exam 100% Pass

  • Exam (elaborations) • 13 pages • 2023
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  • Certified Clinical Research Professional (CCRP) Exam 100% Pass When isn't an IND application needed? IND Application is not needed if investigation does not support change in labeling What information must the general IND include? (21 CFR Part 312.23) FDA Form 1571: -FDA Form 1571 cover sheet -Table of contents -Investigative plan -Investigator's brochure -Protocol -Chemistry/Manufacturing information -Pharmacology/toxicology -Previous human research/literature information -Additional informa...
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CERTIFIED CLINICAL RESEARCH  ASSOCIATE STUDY GUIDE EXAM | 219  QUESTIONS & 100% CORRECT  ANSWERS (VERIFIED) | LATEST  UPDATE | GRADED A+ | ALREADY  GRADED
  • CERTIFIED CLINICAL RESEARCH ASSOCIATE STUDY GUIDE EXAM | 219 QUESTIONS & 100% CORRECT ANSWERS (VERIFIED) | LATEST UPDATE | GRADED A+ | ALREADY GRADED

  • Exam (elaborations) • 60 pages • 2024
  • CERTIFIED CLINICAL RESEARCH ASSOCIATE STUDY GUIDE EXAM | 219 QUESTIONS & 100% CORRECT ANSWERS (VERIFIED) | LATEST UPDATE | GRADED A+ | ALREADY GRADED
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Pearl's Certified Clinical Research Associate 2023/2024 Exam Study Guide (A+ Guaranteed)
  • Pearl's Certified Clinical Research Associate 2023/2024 Exam Study Guide (A+ Guaranteed)

  • Exam (elaborations) • 38 pages • 2023
  • Research correct answers The systematic study of materials and sources in order to establish facts and reach new conclusions. Ethical correct answers Conforming to an established set of principles or accepted professional standards of conduct. Budget development correct answers The process of identifying all of the expenses associated with participating in a clinical trial. Budget negotiation correct answers The process of engaging the sponsor in a dialogue that results in a final budge...
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Certified Clinical Research Professional (CCRP) Exam Study Guide.
  • Certified Clinical Research Professional (CCRP) Exam Study Guide.

  • Exam (elaborations) • 8 pages • 2024
  • Certified Clinical Research Professional (CCRP) Exam Study Guide. When isn't an IND application needed? - correct answer IND Application is not needed if investigation does not support change in labeling What information must the general IND include? (21 CFR Part 312.23) - correct answer FDA Form 1571: -FDA Form 1571 cover sheet -Table of contents -Investigative plan -Investigator's brochure -Protocol -Chemistry/Manufacturing information -Pharmacology/toxicology -Previous human res...
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Certified Clinical Research Professional (CCRP) Exam Already Passed
  • Certified Clinical Research Professional (CCRP) Exam Already Passed

  • Exam (elaborations) • 13 pages • 2023
  • Available in package deal
  • Certified Clinical Research Professional (CCRP) Exam Already Passed When isn't an IND application needed? IND Application is not needed if investigation does not support change in labeling What information must the general IND include? (21 CFR Part 312.23) FDA Form 1571: -FDA Form 1571 cover sheet -Table of contents -Investigative plan -Investigator's brochure -Protocol -Chemistry/Manufacturing information -Pharmacology/toxicology -Previous human research/literature information -Additional in...
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Certified Clinical Research Professional (CCRP) Exam with Answers 2024
  • Certified Clinical Research Professional (CCRP) Exam with Answers 2024

  • Exam (elaborations) • 7 pages • 2024
  • Certified Clinical Research Professional (CCRP) Exam with Answers 2024
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