iVRS has an exceptional track record in clinical site management that ensures scientific excellence and data integrity across all sites. iVRS has highly competent clinical research associates to perform all aspects of site management throughout the study.

Our team of experts exercise ultimate efficiency in managing investigator sites and focus on ensuring adherence to regulatory compliance, protocol adherence, data quality, subject safety, and early resolution of any issues throughout the trial. 

Our experts oversee the data collection, review source documentation and case report forms, ensure regulatory compliance and resolve data queries.

As part of our site management services, we also support the training of site staff to meet industry compliance standards and ensure that the site staff are adequately prepared for audits and inspections.

Our project management team offer the following services under site management:

◘ Site setup and documentation

◘ Regulatory document collection, review & management

◘ Management / facilitation of IRB/EC submissions, query    resolution and till approvals

◘ Site communications and Query resolution

◘ Support Site team on patient recruitment and retention strategies

◘ Training on study protocol, Good Documentation Practices (GDP) and Good Clinical Practice (GCP)