Our Story
A regulatory consultancy born from a deep commitment to public health, scientific integrity, and the growth of Africa's healthcare and consumer goods industries.
To ensure regulatory excellence by guiding clients through every stage of the regulatory process — from strategy development to post-market compliance — delivering exceptional client service through personalized support and long-term partnerships.
To be the leading regulatory affairs consultancy in East and Central Africa — a trusted bridge between innovation and compliance, enabling companies of all sizes to thrive in the region's dynamic healthcare market.
Compliance is not just a requirement — it's a promise. We safeguard patient safety, uphold ethical standards, and empower companies to thrive in Kenya's dynamic healthcare market while aligning with international frameworks.
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. We serve a diverse portfolio — from local startups to multinational corporations entering the East African market.
We work closely with the Pharmacy and Poisons Board (PPB), KEBS, KPRA, and other authorities, ensuring your products meet all local requirements while aligning with international standards such as ISO 13485 and WHO guidelines.
7+ Years · East African Regulatory Affairs
Maryline leads Marsland with a strong focus on compliance, efficiency, and client success. Her expertise covers medical devices, food supplements, cosmetics, pharmaceuticals, and market access strategy across East Africa.
Medical Devices & Pharmaceuticals
Guidance on regulatory requirements and interactions with PPB and EAC authorities for device and pharma submissions.
Technical Documentation
Preparation of CTD/ACTD and authority-specific submissions to streamline approvals and reduce delays.
KPRA · KEBS · KEPHIS
Support for cosmetic notifications, safety assessments, labeling, and claim substantiation across the region.
Compliance & Surveillance
Ongoing monitoring, variations, renewals, and pharmacovigilance/technovigilance to maintain product compliance.
