Our Services
Africlinix Solutions delivers end-to-end clinical research services tailored to sponsors seeking efficient, compliant and ethical trial delivery across Africa.
Strategic Consulting & Feasibility
We support sponsors at the earliest stages of development by providing clear, data-driven insights into the feasibility and risks of conducting trials in Africa.
Our services include:
- Country and site feasibility assessments
- Regulatory pathway strategy (UK HRA/MHRA and African NRAs)
- Protocol optimisation for African clinical and operational contexts
- Operational, ethical and regulatory risk assessments
Commercial model: Fixed-fee project or retainer
Trial Start-Up & Regulatory Management
We manage end-to-end trial start-up activities, ensuring efficient approvals and site readiness across multiple jurisdictions.
Our services include:
- UK and African regulatory submissions and approvals
- Ethics committee engagement and responses
- Site identification, qualification and contracting
- Essential document collection and trial master file support
Commercial model: Milestone-based fees
Clinical Operations
Africlinix provides full clinical operations management through a hybrid UK-Africa delivery model.
Our services include:
- Full trial management and oversight
- Central and local monitoring
- Site management and investigator support
- Vendor and biosample logistics oversight
- Budget, timeline and risk management
Commercial model: FTE or fee-for-service
Specialty & Enabling Services
We offer specialist services to support complex trials and enhance data quality.
Our services include:
- Pharmacovigilance and local adverse event reporting
- Data management and biostatistics
- Quality assurance and GCP audits
- Central laboratory coordination