Latest News

• Intention for Cancellation of Products with Pending Retention Fees

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  Posted On: Jul 26, 2023

• Draft Guidelines for Handling Unfit Medical Devices and Diagnostics

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  Posted On: Jul 19, 2023

• The Use of Antimicrobial Preservatives in Oral Solid Dosage Formulations

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  Posted On: Jun 21, 2023

• New Guidelines for Good Manufacturing Practices (GMP) Inspection of Human Medicinal Products Manufacturing Facilities, 2023

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  Posted On: Jun 16, 2023

• Request for EOI for Shortlisting of Evaluators

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  Posted On: Jun 09, 2023

• Publication of Clinical Trial Public Assessment Reports and GCP Public Inspection Reports

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  Posted On: Jun 02, 2023

• Timelines for Issuance of Clinical Trial Certificates

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  Posted On: May 29, 2023

• Training on Good Regulatory Practices for Stakeholders and Dealers in Medical Devices, Diagnostics and Laboratory Equipment

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  Posted On: Apr 08, 2023

• Uwepo Katika Soko wa Dawa Bandia aina ya Diomycin 250mg, Diodol 500mg, Dioclox 250mg, Mp-Cloxtm 500mg na Indozen 25mg Katika Vifungashio vya Makopo

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  Posted On: Mar 29, 2023

• Reminder to all Sponsors and Principal Investigators

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  Posted On: Jan 24, 2023