Ccrp written exam - Study guides, Class notes & Summaries

CCRP SOCRA Exam - Practice Exam Correctly Answered. 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 - correct answer C) Sponsor What is the minimum number of IRB Members? A) 3 B) 5 C) 6 D) 10 - correct answer 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...

CCRP SOCRA Preparedness baseline Exam knowledge Questions with Expertly written solution 2024/2025 What FDA regulations govern UADE reporting? - correct answer 21 CFR 812 (.15 and .3) What regulations govern research with pregnant women and fetuses? - correct answer 45 CFR 46 Subpart B What requirements must be met to conduct research with pregnant women/fetuses? - correct answer 1) With preclinical and clinical data on non-pregnant women assessing risk to pregnant women 2) Risk to fet...

CCRP SOCRA Exam - Practice Exam 1 with Complete Solutions NB: Answers to questions appear at the bottom of the choices and are highlighted in yellow 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...

CCRP Exam 2024 with 100%Correct Answers. How many days does a sponsor have to report an emergency use of an IP to the FDA? correct answer5 working days How many members must sit on an IRB? correct answer5 How long must an IRB retain records per 21 CFR 56? correct answer3 years after completion of research What are the criteria for IRB approval of research? (7) correct answer1. Risks to subjects are minimized 2. Risks are reasonable in relation to anticipated benefits 3. Selection of subj...

CCRP Exam 2024 with 100%Correct Answers. How many days does a sponsor have to report an emergency use of an IP to the FDA? correct answer5 working days How many members must sit on an IRB? correct answer5 How long must an IRB retain records per 21 CFR 56? correct answer3 years after completion of research What are the criteria for IRB approval of research? (7) correct answer1. Risks to subjects are minimized 2. Risks are reasonable in relation to anticipated benefits 3. Selection of subje...

SoCRA CCRP Test Exam Review Questions with all Answers verified for accuracy Updated 2024/2025 Viable - correct answer as it pertains to the neonate, means being able after delivery to survive. Human Subject - correct answer A living individual about whom an investigator conducting research obtains 1)Data through intervention or interaction with the individual 2) Identifiable private information. (45 CFR, sec. 46.102) Certification - correct answer The official notification by the insti...

CCRP Exam Questions with Complete Solutions A Grade Year/ description of the Nuremberg Code - Answer-1947- German physicians conducted unethical experiments on concentration camp prisoners without their consent. What implications came of the Nuremberg Code? - Answer-Ten elements of human research including voluntary informed consent is absolutely essential. Year and description of the Declaration of Helsinki - Answer-1964- Based on the principles of the Nuremberg code. This declaration...

CCRP SOCRA Exam | 100% Correct Answers | Verified | Latest 2024 Version 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 healt...

SOCRA CCRP Exam 2022 Review with Comprehensive Solutions | Latest 2023/2024 SAE ️ Serious Adverse Event: - results in death - is life threatening (patient was at risk of death at time of the event) - results in persistent or significant disability - congenital anomaly/birth defect Short Form ️ A document that states that the elements of informed consent have been presented orally to and understood by the participant or the participant's LAR. 4 components of short form ️ 1. A shor...

CCRP SOCRA Practice Exam 2024 Final questions and correct answers 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 - CORRECT ANSWER-C) Sponsor What is the minimum number of IRB Members? A) 3 B) 5 C) 6 D) 10 - CORRECT ANSWER-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...