The CRA (Clinical Research Associate),also called clinical monitor, is a health-care professional who performs many activities related to clinical trials. The CRA's task is to check and ensure data quality and regulations, including the Helsinki Declaration, implementation of Good Clinical Practice (GCP) and compliance with the study protocol. Monitoring can significantly improve data quality in clinical studies. Learn about the Visit Frequency with our new video!
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It’s all about the mindset, the GCP-Mindset 💡
