FDA Panel Talk – Research Coordinator’s Point of View – Post Quiz

Which of the following is NOT a key role in a research team conducting FDA trials?

Which training is essential for ensuring ethical conduct in clinical trials?

What is the primary responsibility of a Clinical Research Coordinator (CRC) in an FDA trial?

Which principle of Good Documentation Practice (GDP) emphasizes that records should be created at the time the work is performed?

What is the purpose of conducting mock audits in preparation for FDA inspections?

What does ALCOA-C stand for in the context of documentation practices?

Who is responsible for ensuring compliance with FDA regulations at a clinical trial site?

What is the purpose of maintaining version control in trial documentation?