Archive
Saudi Food and Drug Authority.
Saudi Food and Drug Authority
https://www.sfda.gov.sa/ →Last checked: 13 May 2026 · Last item published: 11 May 2026
113 items archived
-
11 May 2026Reference
Veterinary Products Act and Regulation in GCC
-
11 May 2026Action required
The Registration Rules of Pharmaceutical, Herbal and Health Product Manufacturers and their Products Guideline
Registration rules for pharmaceutical, herbal, and health product manufacturers. -
11 May 2026Action required
The Procedure of Implementing Prices on Pharmaceutical Products
Procedure for implementing prices on pharmaceutical products. -
11 May 2026Awareness
The Policy of Appeal to Drug Sector Decisions
Policy for appealing drug sector decisions. -
11 May 2026Action required
The Implementing regulations of the chemicals import Law
Implementing regulations for chemicals import law. -
11 May 2026Action required
The Implementing Regulations of the Law of Pharmaceutical and Herbal Establishments and Products
Implementing regulations for pharmaceutical and herbal establishments and products law. -
11 May 2026Action required○ Effective 17 September 2020
Requirements to be followed by E-Commerce stores
Requirements for e-commerce stores selling regulated products. -
11 May 2026Action required○ Effective 16 October 2023
Requirements on Importation and Shipments Clearance of Medical Devices (MDS-REQ5)
Requirements on importation and clearance of medical devices shipments. -
11 May 2026Action required
Requirements of Transport and Storage of Pharmaceutical Products Subject to the Supervision of the Drug Sector Through Customs Ports
Requirements for transport and storage of pharmaceutical products through customs. -
11 May 2026Action required○ Effective 24 March 2022
Requirements for the Import and Clearance of Medical Imaging Materials and Particle Accelerators Used in Radioisotopes Formation for Medical Applications (MDS-REQ 4)
Requirements for import and clearance of medical imaging materials and accelerators. -
11 May 2026Action required○ Effective 16 June 2022
Requirements for Unique Device Identification (UDI) for Medical Devices (MDS - REQ 7)
Requirements for unique device identification for medical devices. -
11 May 2026Action required○ Effective 11 January 2026
Requirements for Transporting and Storage of Medical Devices (MDS - REQ 12)
Requirements for transporting and storage of medical devices. -
11 May 2026Action required○ Effective 25 July 2023
Requirements for Safe Use of Medical Devices Inside Healthcare Facilities (MDS-REQ 3)
Requirements for safe use of medical devices inside healthcare facilities. -
11 May 2026Action required○ Effective 28 March 2023
Requirements for Post-Market Surveillance of Medical Devices (MDS - REQ11)
Requirements for post-market surveillance of medical devices. -
11 May 2026Action required○ Effective 19 December 2021
Requirements for Medical Devices Marketing Authorization (MDS-REQ 1)
Requirements for medical device marketing authorization. -
11 May 2026Action required○ Effective 18 August 2022
Requirements for Licensing of Medical Devices Establishments (MDS-REQ9)
Requirements for licensing of medical device establishments. -
11 May 2026Action required○ Effective 11 January 2026
Requirements for Inspections and Quality Management System for Medical Devices (MDS - REQ10)
Requirements for inspections and quality management system for medical devices. -
11 May 2026Action required○ Effective 31 January 2022
Requirements for Importation of Minimally Manipulated Biological Products Intended for Human Application
Requirements for importation of minimally manipulated biological products for human use. -
11 May 2026Action required○ Effective 22 June 2025
Requirements for Clinical Trials of Medical Devices (MDS-REQ 2)
Requirements for clinical trials of medical devices. -
11 May 2026Action required○ Effective 8 January 2026
Requirements for Approval of Technical and Clinical Specifications of Medical Radioactive Materials (MDS-REQ 6)
Requirements for approval of technical and clinical specifications of medical radioactive materials.
Receive these in your inbox each weekday morning.
Subscribe to the brief