The chart shown illustrates the Saudi Arabia approval process and is available for download in PDF format. However, if you would like to explain the steps to someone else in an email, you can cut and paste the text below or send them a link to this page.
The Saudi FDA (SFDA) medical device approval process explained
Prior to being sold in the Kingdom of Saudi Arabia (KSA), medical devices must receive marketing authorization from the Saudi Food and Drug Authority (SFDA) under Interim Regulation (1-8-1429) issued on December 27, 2008.
Your device must have prior market authorization in one of the following reference markets: Australia, Canada, European Union, Japan, or the USA. The device classification in your reference market will determine the classification of your device in the KSA.
Appoint a KSA Authorized Representative (AR) to manage your device registration in Saudi Arabia. Your representative must be licensed with the Saudi Food and Drug Authority (SFDA) and you must have the contract legalized between you and your AR .
Your KSA AR must present the legalized AR contract to the SFDA for review and will obtain a License permitting them to represent you in the Saudi market. You can make the validity of the contract up to 10 years, in which case you only renew every 10 years; however, you still have an annual retention fee every year.
Prepare Medical Device Marketing Authorization (MDMA) application and submit through your AR . The application includes device labeling, IFU, promotional materials, proof of regulatory approval in your reference market and quality system certification (if applicable). Labeling, promotional mat erials and IFU must be in English and Arabic. English only is acceptable for professional use devices. Pay application fee.
The MDMA application is reviewed f or completeness by the SFDA, then passed to a third-party Conformity Assessment Body (CAB) for technical review. The review is rigorous and detailed. Multiple rounds of quest ions are not uncommon.
The SFDA makes the final decision based on recommendations of the CAB. Once the device is approved, the SFDA issues an MDMA certificate and you may begin marketing your device in KSA .
Device registrations are valid for the remaining term of validity in the reference country you have chosen (if there is an explicit expiration date), or three years if the regulatory approval is open ended (example: FDA 510(k) clearance).
Chart updated: 22/06/2017