About us

About Onboard

With ONBOARD, we are leveraging the power of technology to simplify the complex regulatory landscape of the healthcare and life sciences industries in Africa. 

Our mission is to help businesses connect and comply with regulatory standards more efficiently, starting with Nigeria.

Whether registering products, obtaining facility permits, or managing clinical trials, ONBOARD is here to streamline your journey toward full compliance.

Experienced Female consultant

Why Onboard?

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Reduce Delays & Stress:

Regulatory approvals in Africa are complicated and time-consuming. We reduce business disruptions by streamlining regulation.

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Mitigate Risk:

Navigating the evolving regulatory landscape is not just about complying with local laws but also about assessing and mitigating risks. 

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Uphold Safety And Quality:

Upholding product safety and quality assurance standards is necessary to penetrate and scale in the African market

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Scale Across Markets

Maintaining open communication with regulatory authorities allows businesses to adapt to ever-changing local regulations and compliance ambiguity

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Partnership Approach

We view our clients as partners on a shared journey towards improved healthcare access in Africa. We collaborate closely, communicate transparently, and go above and beyond to exceed expectations and deliver value at every step.

Our Team

Our team led by Irene Nwaukwa are healthcare industry experts with over 25 years experience in regulatory compliance, market penetration, business growth & development in healthcare across Africa.

We have a demonstrable history of successfully guiding healthcare businesses through product registration, clinical trial approvals and new product launches using a streamlined process that helps them launch and scale quickly while minimizing risk.

Irene Nwaukwa
Irene Nwaukwa

Founder/ CEO

Healthcare business expert with over 15 years in market penetration, regulatory affairs, business growth & development in healthcare across Africa

Your Trusted Partner for Regulatory Compliance in African Healthcare

FAQs

Find answers to common questions about our services, processes, and how we can help your business succeed.

We operate in Nigeria, Ghana, and Kenya.

The duration of the registration process depends on the timelines set by the regulatory authorities. At Onboard, we ensure efficiency by submitting the required documentation within 7 days of confirmation. We follow up with the regulators on a weekly basis until the permit is issued.

The cost of our services is based on the type of product being registered and the complexity of the process. Factors influencing the cost include whether the product is imported, its classification, required inspections, and the necessary permits.

Yes, we provide comprehensive support for post-registration requirements, including additional services and pharmacovigilance to ensure ongoing compliance and safety monitoring.

Our consultants are highly qualified professionals with extensive experience in the healthcare and regulatory sectors. They hold advanced degrees in fields such as pharmacy, medicine, and regulatory affairs, and have a proven track record of successfully navigating complex regulatory environments.

Still have a questions?

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