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19th Oct, 2024
New Guidelines for Control of Medical Devices and Diagnostics

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

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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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
Unregistered Products

Unregistered prescription medicines pose significant risks to patients because they have not been reviewed by TMDA for safety, effectiveness or quality. Without TMDA review, there is no way to know if these medicinal Products are safe and effective for their intended use, whether they are manufactured in a way that ensures consistent medicines quality. Unregistered medicines may cause patient harm, and TMDA works to protect patients from such Products.
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