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2021-04-01 Extending of work procedures for Medical Device Marketing Authorization (MDMA) requests until the medical device law comes into effect
2021-03-22 Optional issuance of certificate for good manufacturing practice for cosmetics factories and Good distribution and storage practice for pharmaceutical warehouses
2021-03-22 Compliance with SFDA.FD 783 “Instant Coffee”
2021-01-13 Detailed following Announcement (ANNOUNCEMENT 2/13/MDS-AN012)
2020-12-28 extending deadline for receiving requests for marketing authorization applications via GHTF route
2020-09-10 launching medical devices unique device identification (Saudi -DI) system and the Compliance timeframe
2020-08-09 Stop receiving marketing authorization application MDMA via GHTF route
2017-09-25 Fees and Review Times for Authorised Representative Application
2017-09-25 Fees and Review Times for Marketing Authorization Application
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