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Guideline
Year
Format PDF
All Guidelines & Regulations
GUIDELINE TMDA

Guidelines for processing of applications for registration of medicinal products through Non-Routine Procedures

Issuing authority
Tanzania Medicines and Medical Devices Authority (TMDA)
Sector
Medicines, medical devices and diagnostics
Document type
Guideline
Year
Format
PDF · 820 KB
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Guidelines for processing of applications for registration of medicinal products through Non-Routine Procedures was issued by the Tanzania Medicines and Medical Devices Authority (TMDA), which regulates medicines, medical devices and diagnostics. The full text is available above as a PDF (820 KB), free to read and download.

This document is reproduced as published by the issuing authority. For advice on how it applies to your circumstances, speak to our team.