IBBPS sets itself apart in Site Management by offering tailored oversight that ensures strict adherence to Good Clinical Practices (GCP) & Protocols, regulatory compliance, data collection and seamless coordination across diverse clinical trial sites. Our proactive approach and attention to detail guarantee efficient study conduct and superior patient care, surpassing industry standards for quality and reliability. Our processes are as follows:

• Site Identification and Selection
• Site Coordination and Management
• Patient Recruitment and Retention
• Data Management and Quality Assurance
• Regulatory and Ethical Compliance
• Trainings
• Audit and Inspection Preparedness
• IP Handling and Accountability
• Biospecimen Handling, Accountability, and Transportation