This service allows manufacturers and importers of public health pesticides to register their products with the aim of trading, marketing or exporting them.

UDI system (Saudi- DI) aims to record and document the identifier codes for medical devices based on international standards. Device (DI) codes will help the users and stakeholders to recognize all information related to the device through registered UDI codes and labeled on the device package

The Saudi Drug Registration (SDR) System Is an electronic system which aims to facilitate the registration of medicinal, herbal and health products for both Human & Veterinary use

The Electronic Services at the Food Sector It’s an electronic programs designed to build up & develop a database for all establishments of imported or locally produced foodstuff, including names of domestic and foreign food companies, their authorized agents, warehouses, and food products which are licensed and registered in the kingdom of Saudi Arabia.

An electronic system that enables drug companies and agents to upload PIL, SPC, and drug’s picture. It aims to be a reference for registered medicines as a reliable source of drug information

The National Drug & Poison Information Center (NDPIC)

An electronic system that used by the authorized organizations and companies which are dealing with controlled drugs and psychotropic substances. This system links between beneficiaries and the Saudi Food and Drug Authority (SFDA). So, SFDA can control and track controlled drugs and psychotropic substances electronically.

SFDA established Product Classification System for companies to classify their products and get to know the eligibility of products and whether it is subject to registration. The classification exclusively based on the SFDA criteria and products classification guidance. It is an optional service for companies and does not replace registration for other SFDA electronic systems

The Pharmacovigilance Electronic Reporting Service is an online spontaneous reporting system for adverse events and pharmaceutical products defects to facilitate the reporting for health care professionals and the public.​