Clinical Trial Services
Comprehensive end-to-end clinical trial management and regulatory support across Africa
Calebyte BioSolutions
Our Clinical Trial Services division provides comprehensive support for pharmaceutical and biotech companies looking to conduct clinical research across Africa. We combine local expertise with international standards to ensure successful trial outcomes.
Trial Feasibility & Site Readiness
- Comprehensive feasibility assessments for African markets
- Site identification and selection across multiple countries
- Infrastructure assessment and preparation
- Patient population analysis and recruitment strategies
Regulatory Strategy & Submissions
- EFDA (Ethiopian FDA) regulatory submissions and approvals
- USFDA and EMA regulatory alignment
- Multi-country regulatory strategy development
- Ethics committee submissions and approvals
Clinical Trial Management & Monitoring
- Full-service clinical trial management
- On-site and remote monitoring services
- Biostatistics and data management
- Pharmacovigilance and safety reporting
- Local workforce development and training
Why Choose Our Clinical Trial Services
Leverage our deep understanding of African healthcare systems and regulatory environments
Local Expertise
Deep understanding of African healthcare systems, cultural contexts, and regulatory requirements
International Standards
Compliance with ICH-GCP guidelines and alignment with FDA, EMA, and other international standards
Technology Integration
Advanced clinical trial management systems and digital tools for efficient trial execution
Ready to Start Your Clinical Trial in Africa?
Contact our clinical trial experts to discuss your research objectives and regulatory requirements.
Schedule a Consultation