It is an electronic system that provides the service of obtaining halal certificate for establishments including food, drug, cosmetics products and services providers.

The “Opinions” system is a system for requesting the opinion and suggestions of the public, specialists, and concerned parties to express their views on draft regulations, systems, or projects that the SFDA intends to put forward.

A system to receive importing permission requests for infection prevention supplies during COVID-19 pandemic to contribute the provision of products related to the COVID-19 pandemic through the temporary fast track developed by the authority.

Standards web store (mwasfah) is an electronic service enables manufacturers, importers, distributers and consumers, in addition to researchers, specialists and interested personnel subjected to SFDA to access to the Saudi technical regulations and standards in order to meet SFDA provisions and requirements or to guide clients toward achieving or ensuring safety, quality and effectiveness of the products

The leading regional regularity authority for food, drugs and medical devices with proffessional and excellent services that contributes to the protection and advancement of the health in Saudi Arabia

The Drug Sector at SFDA formed up (established) this program to submit the classification applications so the pharmaceutical companies can determine whether their products are registered or not according to the pharmaceutical products classification guideline. procedure is considered to be optional and required. Also, if the product that is classified as (under registration product), the pharmaceutical companies of those products must register their products at SFDA before marketing them.

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.