• Staff Mail
  • Training Opportunities
  • Corporate Customers
  • Vacancies
  • F.A.Q's
  • English Kiswahili
emblem
TMDA building
Logo
ISO 9001 : 2015 CERTIFIED
  • Home
  • About TMDA
    • TMDA Profile
    • TMDA Management Team
    • TMDA Organogram
    • Ministerial Advisory Board
    • Client's Service Charter
    • Business Support
      • Planning, Monitoring and Evaluation Section
      • Human Resources and Administration Section
    • Acts and Regulations
    • Notable Achievements
    • Quality Management System
    • Technical Committees
  • Medicines
    • Medicines Registration
      • Section Profile
      • Regulations
      • Guidelines
      • Application Forms
      • Technical Committee
      • Approved Medicines Product Information and TPAR
      • Registered Medicinal Products
      • Procedures for Marketing Authorization
      • Control of Advertisment and Product Promotion
      • Harmonization and International Collaborations
        • AMA
        • AMRH
        • WHO Collaborative Procedure
        • East African Community Mutual Recognition Procedures (EAC-MRP)
      • Orphan Medicines
    • Medicines Control Inspection and Enforcement
      • Section Profile
      • Regulations
      • Guidelines
      • Forms
      • Guidance
      • Import and Export Control
      • Registered Premises
      • Promotion of Domestic Pharmaceutical Manufacturers
      • List of Authorized Inspectors
      • List of Authorized Ports of Entry
      • GMP Inspection
      • List of Inspections Conducted by TMDA
      • GSDP Inspection
      • GMP Technical Committee
      • Registration and Licensing of of premises
      • Recall of Products
      • Rapid Alert System
      • Public GMP Inspection Reports
      • Disposal of Unfit Products
    • Clinical Trials and Pharmacovigilance
      • Section Profile
      • Clinical Trials
        • Regulations
        • Guidelines
        • Clinical Trial Application Forms
        • Clinical Trials Control
        • Clinical Trial Committee
        • Clinical Trial Reports
        • Online submission of Clinical Trial Applications
        • Import and Export of Investigational Products
        • Post Marketing Surveillance of Medicines
      • Pharmacovigilance
        • Regulations for Pharmacovigilance
        • Guidelines for monitoring safety of medicines and vaccines
        • Reporting of Adverse Drug Reactions (ADRs)
        • Drug Safety Bulletin
        • Pharmacovigilance Projects
        • Vaccine Safety Net
        • Vigilance Technical Committee Members
        • The National Pharmacovigilance Roadmap
      • Harmonization Initiatives on Clinical Trial
    • Unregistered Products
  • Medical Devices and Diagnostics
    • Medical Devices Assessment
      • Section Profile
      • Guidelines
      • Regulations
      • Application Forms
      • Procedures for Marketing Authorization
      • Registered Medical Devices and In-vitro Diagnostics Devices
      • Notified Medical Devices and In Vitro Diagnostics
      • Control of Advertisements and Product Promotions
      • Medical Devices Public Assessment Reports
      • Fees and Charges Regulations
    • Premises Licensing and Compliance
      • Section Profile
      • Regulations
      • Guidelines
      • Import and Export Control
      • Registration and Licensing of Premises
      • Quality Audit
      • Registered Premises
      • Fees and Charges
      • Recall of Devices and Diagnostics
      • Disposal of Unfit Devices and Diagnostics
      • List of Medical Devices and Diagnostics Manufacturing Facilities
    • Vigilance
      • Section Profile
      • Regulations
      • Guidelines
      • Forms and Checklists
      • Safety Performance
      • The Safety and Quality Reporting Tool
      • Post-marketing Surviellance
    • Harmonization and International Collaboration
      • 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
  • Laboratory Services
    • About TMDA Laboratories
    • TMDA Laboratories
      • Dar es salaam Laboratory
      • Mwanza Laboratory
      • Dodoma Laboratory
      • Medicine Quality Assurance Centres
    • Harmonization initiatives
    • Documents
      • Regulations
      • Guidelines
    • Laboratory Technical Committee
    • Research Hub
  • E-Services
    • Online Medicines Registration
    • Import/Export Permits Application System
    • Online Premises Registration
    • Online GMP Application
    • Online Clinical Trials Application System
    • Safety and Quality Reporting Tool
    • Clinical Trial Registry System
    • Pharmacy Council (Registered Facilities)
    • Online Medical Devices Registration
  • News & Events
    • Publications
      • Drug safety bulletin
      • Fact Sheet
      • Strategic Plan
      • Scientific Publications
      • IEC Materials
      • 10 Years Report
      • TMDA Presentations
      • MOU
      • Whistleblowing Policy
    • Newsletters
    • Service Delivery Survey Reports
    • TMDA Libraries
    • Photo Gallery
    • Annual Reports
    • Speeches
    • News
      • Old Public News
      • Public Notice
    • CAG Reports
  • Projects
    • Projects Overview
    • BREEDIME Project
    • AU-3S Programme
    • The Gates Global Grand Challenges
    • Saving Lives and Livelihoods
    • RER-CTO Project
    • Completed Projects
      • ASCEND Project
      • PROFORMA Project
      • PAVIA Project
  • Zone Offices
    • Central Zone
    • Eastern Lake Zone
    • Eastern Zone
    • Northern Zone
    • Southern Highlands Zone
    • Southern Zone
    • Western Lake Zone
    • Western Zone
  • Tobacco
  1. Registered Premises

Latest News

  • Aug 20, 2025
    Matokeo ya Usaili wa Vitendo Kada ya ICT Programmer
  • Aug 11, 2025
    Report of The Controller and Auditor General on The Financial and Compliance Audit for The Financial Year ended 30th June 2024
  • Jul 28, 2025
    Pharmacovigilance Short Course
  • Jul 16, 2025
    JOB VACANCIES
View All

Upcoming Events

View All

Registered Premises

  1. To view list of premises registered by TMDAClick to view
  2. To view list of Premises registered by Pharmacy CouncilClick to view
Logo
Quick Links
  • TMDA intranet
  • TMDA Staff Email
  • Tanzania Trade Portal
  • Mfumo wa kuomba vibali vya kusafiri nje ya nchi
  • East African Community
Contact Info
All correspondents should be addressed to Director General
  • P.O. Box 1253, Dodoma or P.O. Box 77150, Dar es Salaam, Tanzania.
  • Telephone: +255 22 262961989 / 262961990
  • Fax: +255 22 2450793
  • Email Address: info@tmda.go.tz
    • Twitter
    • YouTube
Website Visitors
  • Online : 0
  • Today : 0
  • Yesterday : 0
  • This Week : 0
  • This Month : 0
  • Total : 0 (since 14th August, 2019)
Related Links
  • International Medical Device Regulators Forum (IMDRF)
  • Pharmacy Council (PC)
  • Ministry of Health
  • National Institute of Medical Research, Tanzania (NIMR)
  • World Health Organization (WHO)
  • Sitemap
  • Privacy Policy
  • Terms and Conditions
  • Copy Right Statements.
  • Disclaimer
All Rights Reserved. © TMDA.All Rights Reserved.
The website is designed, developed and maintained by e-Government Authority. Content maintained by Tanzania Medicines and Medical Devices Authority.