SOCRA CCRP Practice Exam

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Master the SOCRA CCRP Exam with our comprehensive practice quiz. Tailored feedback, detailed explanations, and real-world scenarios to boost your confidence and success.

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What is an additional document required during the trial for both investigator and sponsor?

Subject ID list
IP accountability records
Subject enrollment list
Final report to IRB

The correct answer is: IP accountability records

In a clinical trial, an important document that is required by both the investigator and the sponsor is the IP accountability records. This document keeps track of the investigational product, including its dispensing, return, and destruction. Options A, C, and D are not correct because they are not documents required by both parties during the trial. The subject ID list only pertains to the participants, the subject enrollment list is specific to the investigator, and the final report to the IRB is only required from the sponsor.