End-to-End Clinical Trial Management
From site selection to data management — iCTS handles every phase of the clinical trial process with precision, integrity, and empathy.
Site Selection & Investigator Selection
Strategic identification and qualification of optimal trial sites and principal investigators across the US and West Africa.
IRB, Ethics & DSMB
Comprehensive IRB, Ethics Committee, and Data Safety Monitoring Board consultation, review and submission management.
Patient Enrolment
Community-anchored patient recruitment strategies ensuring diverse, representative participation in clinical trials.
Data Management
Rigorous data collection, management and analysis ensuring integrity, accuracy, and full regulatory compliance.
Clinical Monitoring
On-site and remote monitoring services ensuring protocol compliance and patient safety throughout the trial.
Regulatory Affairs
End-to-end regulatory strategy and submission support for IND applications, protocol amendments, and safety reporting.
Grant Programs
Service grant programs designed to support investigators and institutions seeking to advance clinical research capacity.
Community Outreach
Deep community engagement strategies to build trust and ensure sustainable, diverse patient recruitment pipelines.
Scientific Advisory
Access to our distinguished Scientific Advisory Board for guidance on study design, endpoints and scientific integrity.
Ready to get started?
Partner with iCTS for your next clinical trial. We bring expertise, community, and integrity to every engagement.
