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Uganda: NDA Posts New Guide for Introducing a New Formulation Pharmaceutical Products

Wednesday, January 24, 2018: The National Drug Authority (NDA) of Uganda has released guidelines for local pharmaceutical manufacturers on the requirements for pre-manufacture and pre-registration of a pharmaceutical product that they intend to manufacture, register and market in Uganda.

These guidelines apply to all new pharmaceutical dosage formulations that are intended to be manufactured in Uganda and do not apply to new pharmaceutical dosage formulations for manufacturers outside Uganda.

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