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Question 1 of 8
1. Question
Which of the following is NOT a key role in a research team conducting FDA trials?
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Question 2 of 8
2. Question
Which training is essential for ensuring ethical conduct in clinical trials?
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Question 3 of 8
3. Question
What is the primary responsibility of a Clinical Research Coordinator (CRC) in an FDA trial?
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Question 4 of 8
4. Question
Which principle of Good Documentation Practice (GDP) emphasizes that records should be created at the time the work is performed?
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Question 5 of 8
5. Question
What is the purpose of conducting mock audits in preparation for FDA inspections?
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Question 6 of 8
6. Question
What does ALCOA-C stand for in the context of documentation practices?
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Question 7 of 8
7. Question
Who is responsible for ensuring compliance with FDA regulations at a clinical trial site?
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Question 8 of 8
8. Question
What is the purpose of maintaining version control in trial documentation?
