Site Management
IDDCR Global Research provide a wide range of site management services to support clinical trials. These services are crucial for ensuring the efficient and ethical conduct of research
Site Selection and Initiation
Identification of suitable sites: CROs have networks of experienced investigators and institutions to identify sites that align with the study's objectives.
Site feasibility assessments: CROs evaluate sites based on factors such as infrastructure, expertise, and patient population to determine their suitability for the trial.
Site initiation activities: CROs assist in obtaining necessary regulatory approvals, setting up study infrastructure, and training site staff.
Patient Recruitment and Retention
Recruitment strategies: CROs develop and implement effective recruitment plans to attract and enroll eligible patients.
Patient screening and eligibility verification: CROs ensure that patients meet the inclusion and exclusion criteria for the study.
Patient retention efforts: CROs implement strategies to retain patients throughout the trial, minimizing dropout rates.
Study Monitoring and Oversight
Site visits: CROs conduct regular site visits to monitor study progress, ensure compliance with protocols, and address any issues.
Data quality assurance: CROs review and verify data collected at the sites to maintain data integrity.
Regulatory compliance: CROs ensure that the study is conducted in accordance with Good Clinical Practice (GCP) guidelines and applicable regulations.
Data Management and Analysis
Data collection and management: CROs oversee data collection processes and ensure accurate and timely data entry.
Data cleaning and validation: CROs review data for errors and inconsistencies, and take corrective measures as needed.
Data analysis support: CROs may provide assistance with data analysis, including statistical analysis and reporting.
Study Closeout and Reporting
Study completion activities: CROs assist with the completion of the study, including final patient visits and data collection.
Regulatory submissions: CROs help prepare and submit regulatory documents, such as clinical study reports and safety updates.
Archiving and retention: CROs ensure that study records are properly archived and retained in accordance with regulatory requirements.