As part of our participation in GHE 2025, we were pleased to deliver a professional presentation on SFDA Medical Devices (MD) Registration requirements, presented by our Head of Regulatory and Office Manager, Mr. Hamoud Al Sahli.
The session highlighted key regulatory pathways, registration processes, and compliance considerations for medical devices in Saudi Arabia. It provided attendees with practical insights into navigating SFDA requirements and understanding current regulatory expectations.
We appreciated the strong engagement, questions, and discussions from healthcare professionals, manufacturers, and industry partners who attended the presentation. This interaction reflects the growing interest in regulatory readiness and compliant market access within the Kingdom.
We thank everyone who joined our session and visited our booth, and we look forward to continuing to support the healthcare sector with regulatory expertise and guidance.