Clinical Trial Site Monitoring ensures that clinical trials run smoothly and operate in compliance with the responsible regulatory authorities, the protocol, and Good Clinical Practices.
Monitoring provides sponsor oversight into areas such as:
- Participant enrolment and eligibility
- Data management (collection, data entry, data queries, and overall accuracy and precision)
- Protocol adherence
- Participant safety and adverse event management and reporting
- Regulatory compliance
Monitoring is executed based on the Clinical Monitoring Plan and is carried out by our Clinical Research Associates (CRAs) or Clinical Monitors who carry out regular visits to the site throughout the period of the study.
No single approach to monitoring is appropriate for every clinical trial. As such, dicentra offers a range of monitoring services, including:
- On-site monitoring
- Centralized monitoring
- Risk-based monitoring
Each monitoring plan developed by dicentra is specifically tailored to meet each Sponsor’s needs.
Adherence to protocol and participant health and safety are the highest priorities for dicentra and we will work diligently to ensure your clinical trial sticks to its protocol from start to finish.
Contact dicentra today to learn how we can help you fulfill your clinical trial monitoring needs