MedNova Lifesciences

Contact MedNova Lifesciences

Reach our team for regulatory, PV, and clinical support.

Whether you are preparing for a submission, strengthening pharmacovigilance operations, or planning a clinical program, our team is ready to help you move forward with clarity.

Company information

Office Lagos, Nigeria
Business hours Monday–Friday, 8:00 AM–6:00 PM WAT

Why contact us

We respond to new inquiries with a thoughtful, executive-level approach and help clients move from initial questions to practical planning quickly.

Why companies contact MedNova

Companies contact MedNova when they need clarity on regulatory strategy, pharmacovigilance systems, local market access, or clinical development readiness. Our clients often seek support with submission planning, QPPV readiness, safety governance, internal capability building, and the operational details that matter for Nigeria and the wider West African region. Learn more about our training and consulting services, or ask us for the NAFDAC checklist PDF and glossary insights that support inspection-ready pharmacovigilance and regulatory planning.

We can also connect you with glossary definitions for Medical Information, Medical Writing, adverse drug reaction, Good Pharmacovigilance Practice, and Risk Management Plans.

Services offered

We provide integrated advisory services across regulatory affairs, pharmacovigilance, and clinical development. That includes product registration support, pharmacovigilance system setup, local compliance reviews, investigational site readiness, and regulatory intelligence for evolving local requirements.

Our teams also help with dossier preparation, safety reporting workflows, and lifecycle planning so that regulatory strategy is aligned with commercial and clinical objectives.

Response expectations

New inquiries are handled with a detailed intake process to ensure we understand the project scope, timeline, and point of need. You can expect a prompt, structured response from our team that outlines next steps, potential resourcing, and the expertise needed to move forward.

We aim to respond quickly to urgent regulatory, pharmacovigilance, and clinical development questions while also setting the right expectations for a high-quality engagement.

Industries served

MedNova works with international and regional pharmaceutical companies, biotechnology sponsors, medical device organizations, contract research organizations, and public health programmes. We support products ranging from clinical development candidates to marketed medicines and complex regulatory submissions.

Our experience covers pharmacovigilance, regulatory affairs, market access, and clinical operations in regulated African markets.

Contact us for practical support

Whether your need is a simple consultation, full regulatory support, or a deep pharmacovigilance review, contacting MedNova is the fastest way to align your next step with local requirements and commercial objectives. If you are ready to discuss your programme, please complete the form or reach out directly by phone or email.

When to contact MedNova

Contact MedNova when you are preparing a new market entry, need a pharmacovigilance readiness review, or want help translating regulatory requirements into practical operational plans. Our clients often reach out before product registration, before a major submission, or when they need to improve safety reporting in-market.

Typical response process

After receiving your inquiry, our team reviews the details and responds with a summary of next steps, proposed resources, and a recommended scope. We then schedule a discovery call to confirm requirements, clarify timelines, and identify the most efficient engagement model.

Consultation expectations

You should expect a structured consultation that focuses on the issues most important to your project — whether that is QPPV readiness, regulatory strategy, clinical study design, or safety governance. We provide clear recommendations, highlight local risks, and share realistic timelines for delivery.

Industries served

MedNova serves pharmaceutical manufacturers, biotech sponsors, medical device developers, contract research organisations, and public health programmes. Our experience spans clinical trial support, product registration, and pharmacovigilance operations in West Africa.

Frequently asked questions

What types of enquiries do you handle?

We handle enquiries about regulatory submissions, compliance readiness, pharmacovigilance systems, clinical trial planning, and post-market safety management.

How quickly will you respond?

Our team aims to respond to new enquiries promptly, typically within one business day, with a clear outline of the initial next steps.

Can you help if my product is already on the market?

Yes. We support post-market pharmacovigilance, safety reporting, periodic reporting, and ongoing regulatory maintenance for marketed products in Nigeria and Africa.

What information should I provide in the first message?

Please share the product name, regulatory status, planned timelines, and the specific challenge or support area you need. This helps us give you a faster, more accurate response.

Do you offer remote and local support?

We provide both remote and local support where needed, combining digital engagement with local regulatory expertise to meet programme needs in Africa.

How do I follow up after the initial consultation?

After the initial consultation, we provide a follow-up summary and a recommended next-step plan. You can then choose the support model that best matches your programme needs.