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Ukaguzi wa viwanda
List of Inspections Conducted by TMDA
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Madawa
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Clinical Trial Application Forms
Udhibiti wa majaribio ya dawa
Clinical Trial Committee
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Uwasilishaji wa Maombi ya Majaribio ya Dawa kwa Mtandao
Maombi ya kibali cha kuingiza na kutoa nchini bidhaa za uchunguzi
Ufuatiliaji wa ubora wa dawa kwenye soko
Ufuatiliaji wa usalama wa dawa na chanjo
Kanuni za usalama wa dawa
Guidelines for monitoring safety of medicines and vaccines
Reporting of Adverse Drug Reactions (ADRs)
Jarida la Usalama wa Dawa
Miradi
Taarifa za usalama wa chanjo
Vigilance Technical Committee Members
The National Pharmacovigilance Roadmap
Shughuli za Uwianisho wa Taratibu za Majaribio ya Dawa
Vifaa Tiba na Vitendanishi
Tathmini ya Vifaa Tiba
Section Profile
Miongozo
Kanuni
Fomu
Taratibu za Usajili
Vifaa tiba na vitendanishi vilivosajiliwa
Notified Medical devices and InVitro diagnostics
Control of Advertisements and Product Promotions
Medical Devices Public Assessment Reports
Ada na Tozo
Usajili wa Majengo na Udhibiti
Wasifu wa Sehemu
Kanuni
Miongozo
Import and Export Control
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Quality Audit
Maeneno Yaliyosajiliwa
Ada na Tozo
Recall of Devices and Diagnostics
Disposal of Unfit Devices and Diagnostics
List of Medical Devices and Diagnostics Manufacturing Facilities
Vifaa Tiba
Ukurasa wa Sehemu
Kanuni
Kanuni
Fomu na Checklist
Safety Performance
The Safety and Quality Reporting Tool
Post-marketing Surviellance
Uwianisho na Mashirikiano ya Kimataifa
The African Medical Devices Forum (AMDF)
World Health Organization (WHO)
Global Harmonization Working Party (GHWP)
International Medical Device Regulators Forum (IMDRF)
Regulation of Medical Gases
Technical Committee
Huduma za Maabara
Maabara
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Maabara ya Dar-es-salaam
Maabara ya Mwanza
Maabara ya Dodoma
Medicine Quality Assurance Centres
Harakati za ushirikiano
Nyaraka
Regulations
Muongozo
Laboratory Technical Committee
Research Hub
Huduma za Kieletroniki
Online Medicine Registration
Vibali vya kuingiza na kutoa bidhaa nchini
Online Premises Registration
Online GMP application
Online Clinical Trials Application System
Je umedhurika na dawa,vipodozi na vifaa tiba
Clinical Trial Registry
Pharmacy Council (Registered Facilities)
Online Medical Devices Registration
Habari na Matukio
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Jarida la usalama wa dawa
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BREEDIME Project
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RER-CTO Project
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ASCEND Project
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Ofisi za Kanda
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Kanda ya Mashariki
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Southern Highlands Zone
Kanda ya Kusini
Kanda ya ziwa magharibi
Kanda ya Magharibi
Tumbaku
Matukio yajayo
Taarifa kwa Umma
Jan 07, 2026
Call for Comments on the Draft Guidelines for Reliance on Good Manufacturing Practices (GMP) Inspection
Jan 02, 2026
Mwaliko wa Kushiriki Kikao Kuhusu Udhibiti wa Vifaa Tiba na Vitendanishi Vyenye Asili ya Mionzi
Dec 29, 2025
Submission of Applications for Renewal of GMP Compliance for Foreign Manufacturers
Dec 27, 2025
Payment of Annual Retention Fees for the Year 2026
Angalia Zote
Matukio yajayo
Kikao cha Bodi
16th Feb 2026
Arusha
Angalia Zote
Matukio yajayo
Kikao cha Bodi
MAB Meeting...
Soma zaidi
16
th
Feb 2026
Arusha
