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Guideline on Good Review Practices

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  • Create Date November 16, 2023
  • Last Updated November 16, 2023

Guideline on Good Review Practices

This guideline outlines the fundamental principles and processes governing Good Review Practice (GRevP) as applied by the Pharmacy and Poisons Board (PPB) herein referred to as the Board. The Board operates as a semi- autonomous agency under the Ministry of Health regulating the quality, safety, and efficacy of various Health Products and Technologies (HPTs). To achieve its mission, the Board has established policies, guidelines, standard operating procedures and assessment templates for use in the regulation of health products and technologies. This consolidated comprehensive guideline aims to not only streamline evaluation processes but also enhance evaluation practice standards. This guideline seeks to provide clarity to assessors regarding internal procedures within the Board. This an all- encompassing guideline covers critical aspects such as GRevP, strategies for implementation, the structural framework of medicines evaluation and registration, management of the evaluation process, the cultivation of critical thinking during dossier assessment, and the imperative aspect of communication.

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Tony Kemboi

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