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 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.​

The Saudi Clinical Trials Registry (SCTR) is the entity that houses a formal record for all CTs data in Saudi Arabia. It is responsible for ensuring the completeness and accuracy of the information contained in the register, and that the formal record of an internationally agreed minimum amount of information about a clinical trial is published on a publicly-accessible website.

An electronic system which aims to build-up a national database for all drug establishments including local and international companies and manufacturers, agents and wholesale distributors in Saudi Arabia.

electronic system through which requests for approval of technical and clinical specifications for medical radioactive materials for the benefit of medical establishment are received which requested by importer, re-exporter and transporter establishments of these materials, and then approval of technical and clinical specifications is issued, before applying for importing or re-exporting clearance