About VeroMed
VeroMed exists to make market entry into Kenya predictable. We combine regulatory affairs, quality assurance, and intellectual property into a single engagement so nothing falls between disciplines.
Who we are
VeroMed exists to make market entry into Kenya predictable. We integrate Regulatory Affairs, Quality Assurance, and Intellectual Property into a single engagement, providing one point of accountability from market entry through the product lifecycle.
Most entrants into Kenya split those three functions across separate suppliers. The gaps between them are where submissions stall, audits fail, and brand names have to be surrendered.
Our mission
To provide world-class regulatory, quality, and intellectual property support that accelerates market entry, strengthens compliance, and protects brands within Kenya’s evolving pharmaceutical landscape.
Our vision
To shape East Africa’s pharmaceutical industry through trusted compliance, quality leadership, and regulatory integrity.
Our values
Regulatory work is a trust business. These are the standards we hold ourselves to on every engagement, whether it is a single dossier or a multi-year retainer.
Recommendations grounded in regulations, documented risk, and operational reality.
Systems designed to withstand scrutiny, not merely satisfy requirements.
One engagement, one owner, no gaps between regulatory, quality, and IP responsibilities.
Practical solutions matched to your product, risks, and stage of growth.
Supporting compliance beyond approval and throughout the product lifecycle.
Leadership
Dr. Winnie Mamo is a Registered Pharmacist and seasoned Regulatory Affairs, Quality Assurance, and Supply Chain Operations professional with extensive experience navigating Kenya’s pharmaceutical regulatory landscape.
She has led CTD dossier submissions, GxP compliance programs, inspection readiness initiatives, and IP clearance strategies for manufacturers, distributors, and health-system partners.
She established VeroMed to provide clear, compliant, and reliable regulatory support that accelerates market entry and strengthens operational integrity in Kenya — a key gateway to the East African market.
The VeroMed model
PPB requires foreign companies to operate through a licensed Scientific Office or an authorized Local Technical Representative. That obligation can be met in different ways, but for many entrants a Scientific Office provides the most efficient route to compliance.
We act as the designated point of contact with PPB, handling submissions, correspondence, and the compliance obligations that come with them.
No local incorporation, payroll, premises, or statutory filings. You get the regulatory standing without the fixed cost base.
Secure document-handling protocols, controlled access systems, and confidentiality agreements safeguard client information throughout the engagement.
Planning market entry?
A short scoping conversation tells you which PPB pathway applies, what your dossier is missing, and what the realistic timeline looks like.
