Staff Mail
Training Opportunities
Corporate Customers
Vacancies
F.A.Q's
English
English
Kiswahili
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
Publications
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
Medical Devices and In Vitro Diagnostics Application Forms
Content not found
‹
1
›
