Ccrp socra - Study guides, Class notes & Summaries
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CCRP SOCRA Exam - Practice Exam 1 Latest Update Already Passed
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CCRP SOCRA Exam - Practice Exam 1 Latest Update Already Passed 
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 health, safety, or welfare of a subje...
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CCRP SOCRA Exam | 100% Correct Answers | Verified | Latest 2024 Version
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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 health, safety, or welfare of a 
subject 
B) Purported or represented to be for a use in ...
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CCRP SOCRA Exam Graded A+
- Exam (elaborations) • 21 pages • 2024
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CCRP SOCRA Exam Graded A+ 
FDA Part 11 - ANSelectronic signatures are of the same validity as handwritten 
signatures, must provide 2 identifiers and verify identification of signer 
FDA Part 50 - ANSFood and Drugs, and ICF 
FDA Part 56 - ANSIRBs 
FDA Part 312 - ANSinvestigational new drug application 
FDA Part 812 - ANSinvestigational drug exemption 
FDA Form 482 - ANSNotice of inspection 
FDA Form 483 - ANSLetter of investigational observations/citation of 
noncompliance that specifies how lon...
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CCRP SOCRA Exam Graded A+
- Exam (elaborations) • 21 pages • 2024
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CCRP SOCRA Exam Graded A+ 
April 30 1996 - ANSICH GCP Development Date 
Quality - ANSICH Q 
Efficacy - ANSICH E 
Safety - ANSICH S 
Multidisciplinary - ANSICH M 
guidance for industry, consolidated guideance - ANSICH E 6 
Clinical Safety Data Management Definitions and Standards - ANSICH E2A 
Safety pharmacology studies for human pharmaceuticals - ANSICH S7A 
Electronic records, electronic signatures - ANS21 CFR Part 11 
Informed Consent - ANS21 CFR Part 50 
Financial Disclosures - ANS21 CFR Par...
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CCRP Socra Exam With Complete Solutions Latest Update
- Exam (elaborations) • 13 pages • 2024
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CCRP Socra Exam With Complete Solutions Latest Update
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CCRP SOCRA EXAM - PRACTICE EXAM #1
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CCRP SOCRA EXAM - PRACTICE EXAM #1
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CCRP SOCRA PRACTICE EXAM 1 CURRENT UPDATE
- Exam (elaborations) • 14 pages • 2024
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CCRP SOCRA PRACTICE EXAM 1 CURRENT UPDATE...
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CCRP SOCRA Exam - Practice Exam #1 Questions And Answers All Verified
- Exam (elaborations) • 13 pages • 2024
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CCRP SOCRA Exam - Practice Exam #1 Questions And Answers All Verified 
 
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 hea...
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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
- Exam (elaborations) • 10 pages • 2024
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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
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CCRP SOCRA Exam Graded A+
- Exam (elaborations) • 44 pages • 2024
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CCRP SOCRA Exam Graded A+
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