Clinical Monitoring

Our experienced Clinical Research Associates (CRAs) work effectively with sites – on-site or remotely – to ensure the study protocol is followed, informed consent is correctly obtained, adverse events are reported, accurate records are maintained, and study drug or devices are accounted for. 

Our monitoring services include traditional, full-service monitoring as well as risk-based approach. CTC has both office-based and regional CRAs. 

CRA

• Site selection 
• On-site visits including site initiation, routine monitoring visits, and close out 
• Remote monitoring visits 
• Risk-based monitoring 
• Centralized monitoring 
• Monitoring oversight 
• Monitoring strategy 
• Monitoring plan 
• Site Management support to ensure site regulatory compliance and adherence to the clinical study protocol 
• Site training 
• Protocol Deviation Management 
• Co-monitoring visits