What we help you do
Site identification, trial monitoring, regulatory navigation, GCP training, and patient recruitment across Nigerian and West African research sites.
We help sponsors and CROs run high-quality, compliant clinical trials across Nigeria and West Africa. Working within the SFRI global network, we handle the groundwork that usually slows market entry: identifying and qualifying investigator sites, monitoring trials to ICH-GCP standard, navigating NAFDAC and ethics-committee approvals, training site staff, and recruiting and retaining patients. The result is a trial that starts faster, stays compliant, and produces data a global sponsor can trust.
What you get
Our team of skilled doctors, nurses, and specialists bring years of experience and expertise to ensure you receive the highest quality of care. We are dedicated to treating each patient with compassion.
- Qualified, audit-ready investigator sites
- GCP-aligned monitoring and source data verification
- Regulatory and ethics submission support (NAFDAC, NHREC)
- Site staff GCP training
- Patient recruitment and retention planning
Pan-African professional services firm delivering clinical research support, healthcare business development, and commercial solutions to global standards.
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