Core Research Services
CREA-N provides a centralized platform for the seamless execution of clinical trials across Kenya and Rwanda, leveraging harmonized SOPs and expert investigators to ensure data integrity and patient safety.
[01]
Study Management & Execution
Comprehensive oversight of Phase I-IV clinical trials with centralized project management, tailored to negotiate regional regulatory landscapes while maintaining global delivery standards.
[02]
Recruitment & Retention
Deep community engagement through CHPs and CABs ensures rapid recruitment of diverse populations and industry-leading retention rates of 95% or higher.
[03]
Quality & Regulatory Affairs
Support for regulatory submissions and ethics approvals, underpinned by harmonized SOPs and centralized quality assurance systems meeting ICH-GCP standards.
[04]
Safety & Pharmacovigilance
Continuous safety monitoring and proactive surveillance for study participants, ensuring ethical compliance and immediate response to all adverse events.
[05]
Digital Health & Data Management
Advanced EDC systems and proprietary digital registries that streamline trial logistics, patient tracking, and real-time data submission for both sponsors and researchers.
[06]
Site Logistics & Supply Chain
Integrated management of investigational products, medical supplies, and lab logistics across our regional network to eliminate operational friction.
Optimized Site Activation & Trial Delivery
CREA-N provides pharmaceutical and biotech sponsors with a high-performance clinical investigator site network designed for efficiency and ethical excellence.
Rapid Feasibility and Site Activation
Centralized Regulatory Support
Harmonized SOPs and Shared Systems
High Performance Recruitment Efficiency
Integrated Data Quality Management
Empowering Researchers & Institutions
CREA-N provides the clinical infrastructure and scientific oversight necessary to bridge the gap between global standards and local health needs.
Integrated Infrastructure & Systems
Access proprietary digital registries, community engagement tools, and Electronic Data Capture (EDC) systems tailored for Sub-Saharan African site operations.
Scientific Oversight & Ethics
Expert support for Investigator-Initiated Studies (IIS), regulatory submissions, IRB coordination, and localized ethical compliance to ensure high-quality study delivery.
Institutional Capacity Building
Strengthening research ecosystems through clinical trial logistics, GCP-compliant workforce training, and strategic workforce development for sustainable research units.
Empowering Communities Through Ethical Engagement
CREA-N fosters trust and accessibility through dedicated health education and screening programs. By leveraging a robust network of Community Advisory Boards (CABs) and Community Health Participants (CHPs), we ensure that every study is culturally aligned and ethically sound, bridging the gap between clinical excellence and the communities we serve across Sub-Saharan Africa.