Capability Statement
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.
MedNova helps sponsors use practical tools such as the NAFDAC QPPV Compliance Checklist, the downloadable checklist PDF, and targeted training and consulting to align regulatory, clinical, and pharmacovigilance readiness. We also draw on glossary guidance for Medical Information, Medical Writing, Good Pharmacovigilance Practice, and Risk Management Plans.
"One accountable partner from product registration through post-marketing safety."
Why Sponsors Choose MedNova
Local regulatory expertise
Direct, hands-on familiarity with NAFDAC's submission process and requirements.
Integrated across the lifecycle
Regulatory, clinical operations, and drug safety under one accountable team.
Faster execution
Registration and study start-up timelines built around real local processes.
Scalable delivery
From a single registration or study to a multi-country program.
Built for sponsors and the people who lead their programs
Three disciplines, one accountable team
Regulatory Affairs
Registration to lifecycle management.
- Product Registration
- NAFDAC Submissions
- Import Permits
- Regulatory Intelligence
- Lifecycle Management
Clinical Development
Feasibility to study close-out.
- Site Feasibility
- Trial Start-Up
- Monitoring
- Project Management
Pharmacovigilance
Trial safety to post-marketing.
- Local QPPV
- Case Processing
- Aggregate Reports
- Risk Management
- NAFDAC QPPV Compliance
What sponsors are actually choosing
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.
Digital tools behind every engagement
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.
Standards we operate to
Reasoning preview — live
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.