PRA’s monitoring services are second to none. With knowledgeable country experienced professionals in more than 80 countries your site and data will be protected and validated throughout your study. PRA monitors investigator sites across the globe using clinical research associates (CRAs) who receive expert training to:
- Assess sites for ability to conduct study
- Activate sites on completion of start-up activities
- Monitor recruitment, eligibility and informed consent procedures
- Validate and verify data collected at site
- Review IP and accountability records
- Review adverse events and Serious Adverse Event reporting procedures
- Monitor Investigator Site Files
