Free SOCRA SOCRA-CCRP Practice Exams Questions 2026 - TheExamsLabs

Start Preparation with the Latest and Real 100% Free SOCRA Certified Professional SOCRA-CCRP Exam Dumps Questions Practice 2026

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Total 131 Questions | Updated On: May 22, 2026

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Question 1

According to the ICH GCP Guidelines, what is the purpose of source documents?

A : To establish diverse subject enrollment

B : To validate insurance reimbursement

C : To provide a record of subjects investigational medical treatment

D : To validate reports submitted to the IRB/IEC

Answer: C

Question 2

An investigator received an updated investigator's brochure from the sponsor; the update did not include changes related to subject safety. Which of the following parties, if any, is the investigator required to noti

A : The IRB/IEC

B : The Data Safety Monitoring Board (DSMB)

C : The regulatory authority

D : No notification is required

Answer: D

Question 3

A revised protocol added genomic testing to banked tissue samples. Before shipping samples, what must the site do?

A : Execute material transfer agreement

B : Ship under dangerous goods requirements

C : Obtain IRB/IEC approval for revised protocol and ICF

D : Notify enrolled subjects

Answer: C

Question 4

A clinical investigator terminated a Phase IV drug study. In accordance with the ICH GCP Guidelines, which of the following documents should the clinical investigator maintain?

A : The master randomization list

B : The completed subject identification code list

C : The final trial closeout monitoring report

D : The audit certificate

Answer: B

Question 5

A sponsor is permitted to charge for an investigational drug but must provide what documentation?

A : CMS approval letter

B : Orphan product evidence

C : IRB attestation of institutional cost burden

D : Evidence of potential clinical benefit and significant advantage

Answer: D

Page: 1 / 27

Total 131 Questions | Updated On: May 22, 2026

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