CCRP Exam Questions and answers 2023 With Complete Solution Graded and Already Passed.

How many days does a sponsor have to report an emergency use of an IP to the FDA? - CORRECT ANS 5 working days How many members must sit on an IRB? - CORRECT ANS 5 How long must an IRB retain records per 21 CFR 56? - CORRECT ANS 3 years after completion of research What are the criteria for IRB approval of research? (7) - CORRECT ANS 1. Risks to subjects are minimized 2. Risks are reasonable in relation to anticipated benefits 3. Selection of subjects is equitable 4. Informed consent will be sought from subjects or LARs 5. Informed consent will be documented 6. There is adequate provision of monitoring 7. There is adequate provision to protect the privacy of subjects How many days does an IRB have to report a change in registration information due to a change in chairperson or contact? - CORRECT ANS 90 days How many days does an IRB have to inform the FDA that it is reviewing different types of FDA products? - CORRECT ANS 30 days How often must an IRB renew it's registration? - CORRECT ANS 3 years What are the 8 basic elements of informed consent per FDA guidelines? - CORRECT ANS 1. Statement that the study involves research, purpose and expected duration, description of experimental procedures 2. Description of reasonably foreseeable risks 3. Benefits 4. Disclosure of alternative procedures or courses of treatment 5. Confidentiality measures 6. Compensation and treatments available if injury occurs 7. contact information 8. Participation is voluntary and subject may discontinue at any time What are the criteria for involving children in minimal risk research? (2) - CORRECT ANS 1. No greater than minimal risk 2. Assent from kid + consent from parent obtained What are the criteria for involving children in greater than minimal risk research with prospect of benefit? (3) - CORRECT ANS 1. Risks are justified by benefits 2. Relation of anticipated benefit is at least as favorable as that presented by alternative approaches 3. Assent + consent What are the criteria for involving children in greater than minimal risk research with no direct benefit? (4) - CORRECT ANS 1. Risks are minor increase over minimal risk 2. Intervention presents experiences that are reasonable commensurate with normal medical and living situations 3. Intervention is likely to yield generalizable knowledge that is vital 4. Assent + consent Sponsors must report SAEs to the FDA within how many days of discovering the event? - CORRECT ANS 15 calendar days (21 CFR 312.32) Investigators must report SAEs to a sponsor within how many days of discovering the event? - CORRECT ANS Immediately (21 CFR 312.64) 2 | P a g e CCRP