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Package deal for CCRP Exam Questions with 100% Correct Answers | Verified | Updated
Package deal for CCRP Exam Questions with 100% Correct Answers | Verified | Updated
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[Show more]CCRP Definitions Test 100% Solved 
21 CFR 50 - ANSProtection of Human Subjects 
Sponsor - ANSa person who initiates a clinical investigation, but who does not 
actually conduct the investigation 
Sponsor-investigator - ANSan individual who both initiates and actually 
conducts (alone or with others)...
Preview 3 out of 29 pages
Add to cartCCRP Definitions Test 100% Solved 
21 CFR 50 - ANSProtection of Human Subjects 
Sponsor - ANSa person who initiates a clinical investigation, but who does not 
actually conduct the investigation 
Sponsor-investigator - ANSan individual who both initiates and actually 
conducts (alone or with others)...
CCRP Exam Graded A+ 
21 CFR 11 - ANSElectronic Records; Electronic Signatures 
B - Electronic Records 
C - Electronic Signatures 
21 CFR 50 - ANSProtection of Human Subjects/Informed Consent 
B - Informed Consent 
50.23 - Exception from General 
50.24 - Exception from Informed Consent Requirements f...
Preview 4 out of 41 pages
Add to cartCCRP Exam Graded A+ 
21 CFR 11 - ANSElectronic Records; Electronic Signatures 
B - Electronic Records 
C - Electronic Signatures 
21 CFR 50 - ANSProtection of Human Subjects/Informed Consent 
B - Informed Consent 
50.23 - Exception from General 
50.24 - Exception from Informed Consent Requirements f...
CCRP Exam Graded A+ 
How many days does a sponsor have to report an emergency use of an IP to the 
FDA? - ANS5 working days 
How many members must sit on an IRB? - ANS5 
How long must an IRB retain records per 21 CFR 56? - ANS3 years after 
completion of research 
What are the criteria for IRB appro...
Preview 3 out of 29 pages
Add to cartCCRP Exam Graded A+ 
How many days does a sponsor have to report an emergency use of an IP to the 
FDA? - ANS5 working days 
How many members must sit on an IRB? - ANS5 
How long must an IRB retain records per 21 CFR 56? - ANS3 years after 
completion of research 
What are the criteria for IRB appro...
CCRP EXAM WITH VERIFIED 
QUESTIONS AND ANSWERS 
How many days does a sponsor have to report an emergency use of an IP to the 
FDA? - ANS5 working days 
How many members must sit on an IRB? - ANS5 
How long must an IRB retain records per 21 CFR 56? - ANS3 years after 
completion of research 
What are...
Preview 4 out of 41 pages
Add to cartCCRP EXAM WITH VERIFIED 
QUESTIONS AND ANSWERS 
How many days does a sponsor have to report an emergency use of an IP to the 
FDA? - ANS5 working days 
How many members must sit on an IRB? - ANS5 
How long must an IRB retain records per 21 CFR 56? - ANS3 years after 
completion of research 
What are...
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