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

Adverse Reaction Reporting Tool

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

Registered Products

Approved Medicine Product Information

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

Medicine

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 programme establishing acceptable evidence of safety and efficacy before being placed onto the market.