Saudi Drugs information system (SDI)
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
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)
National Center for Medical Devices Reporting ( NCMDR ) A systematic database to manage medical devices' post-market activities, such as Medical devices reporting of Adverse events and complaints, as well as publishing the Safety alerts of Medical devices with follow-up implementation of the corrective actions to ensure the safety, efficacy and performance of medical devices.
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.
It provides many services for the stakeholders, obtaining standards, giving feedback on draft standards, proposing standards, and reviewing draft of standards before publishing
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
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.
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.