Your Regulatory & Clinical Development Partner for Nigeria and Africa
Integrated regulatory affairs, clinical development, and drug safety services supporting sponsors across Nigeria and West Africa.
"One accountable partner from product registration through post-marketing safety."
Direct, hands-on familiarity with NAFDAC's submission process and requirements.
Regulatory, clinical operations, and drug safety under one accountable team.
Registration and study start-up timelines built around real local processes.
From a single registration or study to a multi-country program.
Registration to lifecycle management.
Feasibility to study close-out.
Trial safety to post-marketing.
Direct NAFDAC experience — hands-on familiarity with how NAFDAC's submission process and documentation standards actually work in practice.
Integrated across the product lifecycle — registration, trial operations, and drug safety under one accountable team, so continuity isn't lost between vendors.
Locally grounded — direct familiarity with Nigeria's regulatory and site landscape, not a template applied from elsewhere.
Scales with the sponsor — from a single registration or study to a multi-country program.
MedNova uses proprietary digital tools to improve regulatory workflows, pharmacovigilance operations, and clinical trial execution — with a qualified team member reviewing every output. Technology supports the work; it doesn't replace the judgment behind it.
A genuine, working preview of the reasoning behind our process, across regulatory, clinical, and safety disciplines.
Not connected to any client's real data, and not a substitute for a full assessment by our team.