News, Events & Insights
Stay current with SFDA regulatory updates, meet our team at leading healthcare events, and read practical guidance from our specialists.
Global Health Exhibition 2026
Meet the 360SFDE team at the Kingdom's flagship healthcare event. Book a slot to discuss your SFDA registration and market-access strategy.
Upcoming events
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News & announcements
From the blog
Expert guidance on SFDA regulation
SFDA Authorized Representative: requirements & how to appoint one
Foreign manufacturers cannot market devices in Saudi Arabia without a licensed AR — here's the full picture.
The SFDA drug approval framework, explained
A plain-language overview of registration pathways, timelines, and what reviewers expect.
Understanding MDMA: Medical Device Marketing Authorization
The core steps to secure your MDMA and legally market devices in the Kingdom.
ISO 13485 essentials every manufacturer should know
The quality-system foundations that make SFDA submissions smoother and audits easier.
Comparing SFDA's IVD framework with global standards
How Saudi IVD requirements line up with international expectations.
Saudi Vigilance & post-market surveillance basics
What ongoing obligations look like once your product is on the market.
Have a regulatory question?
Talk to a 360SFDE specialist and get a clear answer on your SFDA pathway.