Pharmacovigilance
Structured drug safety support for case processing, signal evaluation, reporting readiness, and lifecycle oversight.
- Signal detection
- ICSR handling
- Risk management support
- QPPV readiness
Services hub
Specialist support for pharmacovigilance, regulatory affairs, clinical development, and compliance in Nigeria and Africa.
MedNova brings multidisciplinary expertise across drug safety, regulatory consulting, clinical operations, medical writing, and quality assurance to help clients move from complexity to confident execution.
A practical services hub for regulated life sciences programs
MedNova supports sponsors, manufacturers, importers, and healthcare organizations with integrated expertise spanning regulatory experience, scientific execution, compliance readiness, and long-term operational support. We also offer targeted training and consulting to help teams adopt those processes, maintain them beyond the initial engagement, and prepare for NAFDAC review with our Compliance Checklist and downloadable checklist PDF. See glossary guidance for Good Pharmacovigilance Practice and Risk Management Plans to connect compliance and operations more clearly.
Core capabilities
Each engagement is shaped around your product, market, and stage of growth — from early registration planning to ongoing post-marketing oversight.
Regulatory Affairs
Submission strategy, dossier preparation, and local regulatory support for market entry and lifecycle management.
- Regulatory consulting
- NAFDAC submissions
- Import permits
- Renewals and variations
Clinical Development
Operational guidance for trial planning, feasibility, site readiness, and execution across Nigeria and West Africa.
- CRO support
- Study readiness
- Clinical operations
- Regional delivery
NAFDAC Product Registration
Practical support for registration pathways, documentation readiness, and submission discipline.
- Product registration
- Regulatory intelligence
- Submission preparation
- Compliance alignment
Medical Information
Reliable response support for medical inquiries, scientific communication, and cross-functional information flow.
- Medical inquiry support
- Scientific response readiness
- Stakeholder communication
- Region-specific support
Medical Information glossary definition
Learn MoreMedical Writing
Clear, compliant documentation support for scientific and regulatory content development.
- Clinical documents
- Regulatory writing
- Scientific content
- Stakeholder-ready drafts
Medical Writing glossary definition
Learn MoreQuality Assurance & Compliance
Operational quality support that strengthens documentation discipline, readiness, and assurance processes.
- QA support
- Inspection readiness
- Control framework
- Compliance oversight
Post-Marketing Surveillance
Support for ongoing monitoring, signal review, and sustained safety oversight after launch.
- Post-marketing safety
- Signal review
- Reporting support
- Lifecycle monitoring
Regulatory Intelligence
Guidance on changes in requirements, evolving expectations, and best-practice implementation.
- Requirement tracking
- Landscape monitoring
- Strategic guidance
- Commercial readiness
Training & Consulting
Targeted advisory support, capability building, and practical guidance for internal teams and partners.
- Training delivery
- Capability building
- Workflow support
- Executive advisory
Resources & Insights
Explore practical guidance, articles, and knowledge resources that support your team across regulatory, safety, clinical, and quality operations.
Why choose MedNova
Our approach is grounded in regulatory depth, scientific clarity, and dependable delivery from first consultation through ongoing support.
Regulatory Expertise
Practical guidance aligned with local and international expectations for market access and lifecycle management.
Scientific Excellence
Cross-functional support delivered with strong scientific judgment and a methodical operating approach.
Compliance
Documentation discipline and readiness support that help teams prepare with more clarity and confidence.
Fast Response
Responsive support for time-sensitive regulatory and safety needs without losing quality or detail.
Quality Assurance
Structured quality support designed to strengthen processes, oversight, and audit readiness.
Industry Experience
Work across pharmaceuticals, biotechnology, medical devices, nutraceuticals, cosmetics, and healthcare.
Our process
A clear path from consultation through execution, compliance, and ongoing support.
Consultation
We clarify your objective, timeline, and operational context.
Strategy
We define the right path for regulatory, scientific, and compliance requirements.
Execution
We coordinate workstreams with attention to quality, speed, and accountability.
Compliance
We help teams stay inspection-ready and aligned with current expectations.
Ongoing Support
We remain available for follow-through, updates, and evolving program needs.
Industries we serve
Our support is adapted to the operating realities of each sector we work with.
Pharmaceutical
Support for registration, safety, quality, and lifecycle demands across regulated product portfolios.
Biotechnology
Flexible support for innovation-driven programs that need both scientific rigor and regulatory clarity.
Medical Devices
Practical guidance for market access, documentation, and compliance-related execution.
Nutraceuticals
Support for product positioning, documentation, and regulatory alignment in complex categories.
Cosmetics
Targeted guidance for product compliance and market readiness in regulated consumer categories.
Healthcare
Collaborative support for organizations operating across clinical, quality, and market access requirements.
Consultation
Let’s shape a path that supports compliance, speed, and confidence.
Whether you need immediate support or a long-term partner, MedNova can help you map the right next steps for your service needs.
Book a Consultation