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Who we help

Built for companies that answer to regulators

From a first product registration to a mature safety system, we work with the people responsible for compliance.

A pharmacist explaining a medicine to a customer

Who we work with

Our clients

Local manufacturers

Kenyan manufacturers registering new products, keeping registrations current and running pharmacovigilance for their portfolio.

International manufacturers

Companies outside Kenya that need a local technical representative and a qualified person for pharmacovigilance in the country.

Importers and distributors

Marketing authorisation holders and distributors who must report adverse events and keep safety records.

Medical device companies

Registration and post-market safety monitoring for medical devices and in-vitro diagnostics.

Herbal and complementary products

Registration and safety obligations for herbal, complementary and alternative medicines.

Hospitals and programmes

Pharmacovigilance training and safety reporting support for facilities and health programmes.

How we start

What working with us looks like

  1. Step 1

    Discovery call

    A free 30-minute call about your products, markets and deadlines.

  2. Step 2

    Gap assessment

    We review your dossiers or safety system against current requirements.

  3. Step 3

    Written proposal

    Scope, timeline and fees agreed in writing before work starts.

  4. Step 4

    Delivery

    One named lead, regular updates, and support when the regulator asks questions.

Not sure where you fit?

Tell us about your products and we will point you to the right service.