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
Import and Export of Investigational Pharmaceutical Product
IP Handling and Accountability
Biospecimen Handling, Accountability, and Transportation
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INSTITUTE OF BIOLOGICAL, BIOCHEMICAL & PHARMACEUTICAL SCIENCES (IBBPS)