What must researchers ensure before starting a clinical trial?

Prepare for the CITI Good Clinical Practice (GCP) Exam with comprehensive questions, hints, and explanations. Master the essential concepts to excel in your exam!

Before starting a clinical trial, it is essential for researchers to ensure that they have obtained the necessary regulatory approvals and funding. This is critical to ensure that the trial is conducted ethically and in compliance with applicable laws and regulations. Regulatory approvals typically ensure that the study design is adequate, the safety of participants is prioritized, and that the researchers are following Good Clinical Practice guidelines.

Funding is also a crucial aspect because it provides the financial resources needed to carry out the study, including participant recruitment, data collection, and analysis. Without these approvals and funding in place, the trial cannot proceed legally or effectively, which ultimately impacts the integrity and validity of the research findings. Therefore, obtaining necessary regulatory approvals and securing funding create a solid foundation for conducting a successful clinical trial.

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