Authorized Representative in Nairobi, Kenya
We simplify compliance for medical devices, pharmaceuticals, cosmetics and food supplements — so you can focus on innovation and growth.
Marsland Services Limited is a specialized regulatory affairs consultancy providing end-to-end support to companies in the medical devices, pharmaceuticals, cosmetics, and food supplements sectors. We assist organizations in navigating complex regulatory environments across East Africa, ensuring compliance while accelerating market entry.
Our team combines technical expertise with practical industry experience to deliver tailored solutions that align with each client's commercial and regulatory objectives — from strategy development all the way to post-market compliance.
Learn about our team →We provide expert regulatory support across the full product lifecycle — from initial strategy to ongoing post-market compliance.
We provide expert guidance on regulatory requirements, ensuring seamless interaction with regulatory authorities and compliance with applicable standards across East Africa.
Learn more →We work closely with clients to design effective market access and regulatory strategies that support business growth and product lifecycle management across the region.
Learn more →Our team ensures accurate, complete, and timely preparation of regulatory submissions to minimize delays and facilitate approvals with PPB, KEBS, KPRA, and other authorities.
Learn more →We offer ongoing support including compliance monitoring, variations, renewals, and pharmacovigilance/technovigilance activities to keep your products in good standing.
Learn more →Kenya's growing life sciences ecosystem demands a regulatory partner who understands the unique compliance landscape for laboratory instruments, diagnostic reagents, biotechnology tools, and research consumables. Marsland Services Limited brings specialised expertise to this fast-moving sector — helping distributors, manufacturers, and research institutions navigate registration with the Pharmacy & Poisons Board and align with WHO and EAC standards.
From IVD reagent registration to import permit management for research equipment, we streamline every step so your laboratory products reach scientists, clinicians, and researchers without unnecessary delays.
We assess your product, target market, and regulatory requirements to build a tailored compliance roadmap.
Our experts compile and review all technical files, safety data, and supporting evidence required by regulators.
We interface directly with regulatory bodies — PPB, KEBS, KPRA — managing submissions and responding to queries.
We secure your approvals and guide you through launch, including post-market compliance monitoring.
Deep understanding of regional regulatory frameworks and international standards across medical devices, pharmaceuticals, cosmetics, and food supplements.
Customized services designed to meet the unique needs of startups, SMEs, and established organizations — not a one-size-fits-all approach.
A strong track record of successful approvals and satisfied clients across East Africa, from local startups to international organizations.
Flexible service models that reduce operational overhead and provide predictable regulatory costs — maximizing value at every stage.
Efficient processes that shorten timelines from submission to approval, so your products reach the market faster.