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Online services

As we look forward in ensuring quick and effient services to cutomers, we have much utilized to electronic systems that play a big role in implementing Client service charter. Information and services provided over the Internet are as follows below

Import and Export Permit Application

Import and Export Permit Application
Medical Devices Registration

Medical Devices Registration
Medicines Registration

Medicines are registered to ensure that they can bring about the desired therapeutic effects without causing harm to the consumer
Clinical Trial Registry System

Clinical Trial Registry System
Whistleblower Reporting Form

The act of telling TMDA about any violation of law, regulations, or threat to public interest/national security as well as fraud and corruption
Safety and Quality Reporting Tool

This system coordinate reporting of reactions caused by medicines/medical devices and vaccines

ADVERSE DRUG REACTIONS (ADRs) / ADVERSE EVENTS / QUALITY DEFECTS REPORTING

A: PAPER BASED MEANS OF REPORTING

Form 1
Form 2
Form 3
How to Report?
  • Dully fill in the form as required
  • Use a separate form for each patient
  • Report directly to the authority:

Mail:
Tanzania Medicines and Medical Devices Authority,
P.O. Box 1253, Dodoma
P.O. Box 77150, Dar es Salaam, Tanzania.

Fax: +255 22 2450793

Email: clinicaltrials@tmda.go.tz

ELECTRONIC MEANS OF REPORTING

Choose any of the following convenient ways to report ADR/AEFI

Report by Web-Based Application

Browse sqrt.tmda.go.tz from your computer or mobile phone

Web Reporting
Report by Text Message (USSD)

Dial *152*00# on your mobile phone

USSD 1
USSD 2
Report by Mobile App

Install the SQRT App on your mobile phone

Mobile App Reporting

Registered Products

As we look forward in ensuring quick and effient services to cutomers, we have much utilized to electronic systems that play a big role in implementing Client service charter. Information and services provided over the Internet are as follows below

Approved Product Information

Approved product information are published to promote openness and transparency in medicines regulation and build the publics’ confidence
Medicines

Medicines are registered to ensure that they can bring about the desired therapeutic effects without causing harm to the consumer
Medical Devices and Diagnostics

Medical Devices and Diagnostics

TMDA Guidelines

One of the means for ensuring that medicinal products meet the required standards of quality, safety and efficacy is by conducting product specific pre-marketing assessments to determine whether the product should be registered.

CTP Guidelines

Every medicinal product must have satisfactorily completed a clinical trial establishing acceptable evidence of safety and efficacy before being placed onto the market.
Medical Devices and In Vitro Diagnostics Guidelines

Helping health care providers diagnose and treat patients and helping patients overcome sickness or disease, improving their quality of life.
Medicines Guidelines

A document with the aim of guiding decisions and criteria regarding diagnosis, management, and treatment in specific areas of healthcare.
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Customer Feedback

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You can also send complements, complaints or enquiries through the government portal that will make follow-up on about your comments so as to increase public satisfactory.

Please click here, to visit the portal
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