Consulting Services
Conducting clinical trials in Africa comes with immense opportunity but also with unique regulatory and operational challenges. At AfriTrials Connect, our Consulting Services are built to support sponsors, Contract Research Organizations (CROs), and trial investigators through every step of setting up and running compliant, efficient, and successful clinical research projects across the continent.
What We Provide
Regulatory Strategy & Guidance
- We help you navigate national regulatory authority (NRA) requirements, ethics committee approvals, and submission timelines across African countries.
Trial Start-Up Optimization
- From site selection to investigator onboarding, we streamline early-phase planning to reduce delays and avoid compliance pitfalls.
Protocol Review & Localization
- Our experts provide feedback to align your protocol with local cultural, clinical, and regulatory contexts ensuring faster approvals and better community engagement.
Investigator & Site Engagement
- We connect you with local experts, support feasibility planning, and help you build strong site relationships.
GCP, SOP & Quality Compliance Support
- Ensure your trial meets Good Clinical Practice (GCP), ICH, and local regulations with guidance on site readiness, documentation, and monitoring strategies.