Bring your medical device to East Africa
JATESA simplifies regulatory pathways, accelerates approvals, and ensures long-term compliance so your products reach patients faster and with confidence.
Wondering how we simplify your submission?
We act as your Local Representative, handling registrations with the Kenya PPB so you don't have to.
Regulatory experts who know East Africa's pathways
Our team pairs 15+ years of global regulatory experience with hands-on knowledge of PPB and East African submissions, so you get guidance that works on the ground.
J. Ateka
Founder & Principal Consultant
J leads JATESA with 15+ years of international regulatory experience across EU MDR, FDA, LATAM, and APAC markets, now focused on East Africa.
Daniel Ochieng
Senior Regulatory Affairs Advisor
Daniel supports dossier preparation and PPB submissions, helping clients meet requirements across Kenya, Uganda, and Tanzania with clear, step-by-step guidance.
Trusted by Regulatory Leaders.
Our clients consistently achieve streamlined regulatory approvals and market access through our expert guidance and strategic support.
JATESA's guidance with the Kenya PPB made our registration process straightforward.
Daniel Kimathi
Regulatory Affairs Manager, Diagnostic Manufacturer
The multi-country submission across East Africa saved us months of guesswork.
Amara Osei
Quality & Compliance Director, IVD Startup
We finally found a partner who understands both EU MDR and East African requirements.
Jonathan Meyer
VP Regulatory Affairs, Medical Device Company
15+ years of regulatory experience, ready for your dossier
Partners trust us to navigate PPB and East African submissions. Let's map your registration step by step, from dossier to post-market compliance.