Our CRAs offer a high level of quality and consistency in Phase I-IV clinical study monitoring and site management involving drugs, and medical devices. Monitoring services include 100% source document verification and comprehensive and timely site visit reports.CRAs are thoroughly trained in ICH GCP, and regulations. Between monitoring visits, CRAs will keep follow up patient enrollment status and
study progress, provide site support to site personnel to answer protocol questions and discuss CRF completion. CRA will ensure all queries have been resolved and provide appropriately assistance.