We focus on medical product and device registration and conformity, and represent overseas manufacturers before SFDA across four core sectors.
From simple devices to more complex systems — we support classification, regulatory pathway selection, and technical file preparation before MDMA submission.
Related service →Reviewing registration requirements and preparing the data and documents needed before submission to SFDA platforms.
Related service →For technically-regulated products that require a conformity certificate before import or market placement in Saudi Arabia.
Related service →Manufacturers outside the Kingdom who need a licensed local point of contact before SFDA to follow their regulatory obligations.
Related service →Share your product details and we'll help you identify the right regulatory pathway.
