Regulatory Affairs
Product registration
Registration of medicines, medical devices and health products with the Pharmacy and Poisons Board and other East African regulators, including EAC joint assessment where it applies.
Related services
Registration dossiers
Dossiers in the Common Technical Document (CTD) format, checked against current guidance before submission.
Variations and renewals
Changes and renewals filed on time so your registration never lapses.
Local technical representative
A Kenya-based representative for manufacturers outside Kenya, as the Pharmacy and Poisons Board requires.