At Kadesh Sciences International (KSi), we provide high-quality, end-to-end support for clinical trials and health research. Our services are designed to help sponsors, investigators, and institutions achieve excellence in research implementation while maintaining the highest ethical and regulatory standards.
Linking Sponsors to Competent Local Investigators
We connect global and regional sponsors with experienced local investigators who have a proven track record in conducting clinical trials. Our network of experts ensures that studies are managed by qualified professionals familiar with local healthcare systems, cultural contexts, and regulatory requirements.
Access to Relevant Study Participants
KSi facilitates access to diverse patient communities, ensuring efficient recrutiment and retention of study participants. By leveraging our community networks and partnerships with healthcare facilities, we help sponsors reach their target sample size while maintaining inclusivity and ethical engagement.
Clinical Trial Monitoring
We provide robust trial monitoring services to ensure that all studies comply with Good Clinical Practice (GCP), ethical standards, and regulatory requirements. Our monitoring includes trial oversight, data verification, and risk-based monitoring approaches to guarantee data integrity and participant safety.
Ethical and Regulatory Consulting
Our team supports sponsors and investigators in navigating complex ethical and regulatory processes. We provide expert guidance for preparing submissions, obtaining approvals, and securing authorisations from Institutional Review Boards (IRBs), Ethics Committees, and the regulatory authority.
Training and Capacity Building
KSi is committed to strengthening research capacity by providing training programs for investigators, trial coordinators, and clinical teams. Our capacity building initiatives cover GCP, trial management, data handling, and other clinical skills needed to conduct world-class research.
Trial Site Set-up & Protocol Implementation
We provide end-to-end support in establishing and managing trial sites, including infrastructure set-up, staff training, and implementation of research protocols. Our team ensures that all sites are prepared to deliver high-qualtiy studies from initiation through to close-out.
“The quality is outstanding, and the attention to detail is impressive.”
— Chisome Chieme AZIN-V Coordinator
Partners
IVON-PP, AZIN-V Studies
Providing monitoring oversight for two clinical trials implemented by the University of Lagos Teaching Hospital, namely IVON-PP and AZIN-V studies.
Research Alliance Network
Providing consulting services for the Research Alliance Network to set up clinical trial sites in Nigeria, including ethical and regulatory support.
Networking with Global Researchers
Kadesh Sciences International 