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IMPLEMENTATION OF REGULATORY FEES UNDER THE PHARMACY AND POISONS (REGISTRATION OF HEALTH PRODUCTS AND TECHNOLOGIES) RULES, 2022

The Pharmacy and Poisons Board (hereinafter "the Board" is the National Medicines Regulatory Authority established under the Pharmacy and Poisons Act, Cap 244, Laws of Kenya (hereinafter "the Act" with the primary mandate to ensure the quality, safety, and efficacy of Health Products and Technologies.

Pursuant to section 3A (g) of the Act, the Board is empowered to levy, collect, and utilize fees for services rendered. Furthermore, the Board, through the Second Schedule of the Pharmacy and Poisons (Registration of Health Products and Technologies) Rules, 2022, has prescribed a structured schedule of fees applicable to the registration of health products and technologies. These fees are intended to facilitate the effective discharge of the Board's regulatory functions, enhance service delivery, and strengthen public health safeguards.
The Board is currently developing the necessary modalities to ensure the full implementation of the prescribed fees. The same involves developing administrative, operational, and technical measures to support a smooth transition to the full implementation of the fee framework.

In light of the foregoing information, you are hereby notified that the Board will fully transition to the full implementation of the applicable fee schedules as provided under the said second schedule of the Pharmacy and Poisons (Registration of Health Products) Rules, 2022, starting 1st January 2026.

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