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Monitoring activities include pre-study site identification, study initiation, monitoring, drug accountability and site closure. Our monitors are physicians trained in ICH-GCP and EU and local requirements with very good spoken and written English. These factors as well as 100% source data verification ensure high professional standarts and superior data quality. Co-monitoring visits performed by our Quality assurance manager and project managers additionally contribute to the highest level of GCP and protocol compliance.

 

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