Kenya — Regulatory Overlay¶

This folder contains Kenya-specific additions to the general GMP baseline. Each note in this folder is an overlay: it states only what is additional or different for Kenya and links back to the general note it extends.

Do not restate the general baseline here. If a topic applies everywhere, it belongs in 10-general/ only.

Regulatory framework¶

TODO — Do not invent regulations. Before adding any Kenya-specific content, verify the applicable legislation and guidance documents and cite them in the sources field of each note. Key agencies to research:

Kenya Bureau of Standards (KEBS) — national standards body

Pharmacy and Poisons Board (PPB) — cosmetics product notification/registration

Kenya Drug Authority (KDA) — check applicability for food supplements

East African Community (EAC) standards — regional harmonisation may apply

Sections with Kenya overlays¶

None yet. Add links here as country-specific notes are created in this folder.

Topics likely to need Kenya overlays¶

When Kenya-specific notes are created, they will typically cover:

Product notification or registration requirements before sale
Local labelling rules (language requirements, mandatory statements)
Import and export documentation and permits
Local authority inspection expectations and frequency
Any EAC regional standards that differ from ISO 22716

Each new note must link back to the relevant 10-general/ note it extends using the related field and a [[wikilink]] in the body.