WCT's extensive experience in conducting clinical trials, highly trained CRAs, thorough knowledge of local regulations and GCPs, access to cutting edge study management tools and the latest data transmission technology guarantee effective and efficient management of investigator sites.

• Site identification process
• Site selection and qualification visits
• Initiation, interim and study closure visits
• Regulatory document review, collection and processing
• Obtaining local ECs/IRBs approvals
• Site GCP and mentoring/training visits
• Carefully instituted Corrective and Preventive Action Plans (CAPA)
• Query Resolution
• Blinded and unblinded clinical trial material accountability
• Clinical site management via frequent and clear communications
• Subject recruitment oversight
• Study progress monitoring at site
• Mass mailing/Newsletters