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• Submission of Appointment of Qualified Person for PharmacoVigilance (QPPV)

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  Posted On: Sep 27, 2022

• Uploading Pictures and/or Images of Commercial Samples Submitted in Support of Applications for Registration and Re-Registration of Medicinal Products

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  Posted On: Aug 24, 2022

• Uwepo Katika Soko wa Sigara aina ya BHARATH SPECIAL BEEDIES ambayo Haijatambuliwa wala Kusajiliwa na TMDA

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  Posted On: Aug 22, 2022

• Request for EOIs for Shortlisting Evaluators of Medicines

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  Posted On: Aug 03, 2022

• New Guidelines on Applications for Notification of Medical Devices and In Vitro Diagnostic Devices, 1st Edition, 2022

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  Posted On: Aug 01, 2022

• New Guidelines on Applications for Changes to Registered Medical Devices and In Vitro Diagnostic Devices, 1st Edition, 2022

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  Posted On: Aug 01, 2022

• Usajili wa Vitendanishi kwa Kushirikia na Shirika la Afya Duniani (WHO) (Collaborative Registration Procedure (CRP)

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  Posted On: Jul 27, 2022

• Registration of In Vitro Diagnostic Devices (IVDS) Under the Collaborative Registration Procedure (CRP) Pathway

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  Posted On: Jul 27, 2022

• Kuhuisha Usajili na Utambuzi wa Vifaa Tiba na Vitendanishi

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  Posted On: Jul 14, 2022

• Re-Registration and Re- Notification of Medical Devices And In Vitro Diagnostic Devices

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  Posted On: Jul 14, 2022