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Whether you have a specific project or just want to understand your regulatory options — we're here to help. Reach out and we'll respond within 24 hours.
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UNIPEN Flats,Hurlingham
Nairobi, Kenya
Monday – Friday: 8:00am – 5:00pm EAT
Saturday: 9:00am – 1:00pm
Absolutely. We work with companies of all sizes — from individual entrepreneurs launching their first product to large multinational corporations. We tailor our approach and scope to fit your budget and stage of business.
Timelines vary significantly by product category and authority. Cosmetic notifications can be relatively quick (1–3 months), while medical device registration with PPB can take 6–18 months depending on risk class. We provide realistic timeline estimates during your initial consultation.
Yes. We assist with export regulatory documentation including Certificates of Free Sale (CFS), GMP certificates, and export health certificates. We also advise on regulatory requirements in destination markets across East and Central Africa.
To start, we typically need basic product information: product name and type, intended use, country of manufacture, existing test data (if any), and your target market. We'll guide you on everything else during your initial consultation.
Yes. Many clients retain us on an ongoing basis for post-market compliance support, renewal management, regulatory monitoring, and to serve as their local regulatory representative. Contact us to discuss retainer arrangements.