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 Site Initiation Visit SIV with our new video!
For more insight into our world of Clinical Research, and to be sure not to miss a thing,
Visit us on Instagram: / gcpservice
Tweet with us on: / gcpservice
LinkedIn: / gcp-service-internatio...
Xing: www.xing.com/pages/gcp-servic...
Or even visit our Homepage: www.gcp-service.com/
It’s all about the mindset, the GCP-Mindset 💡