← Back to the brief
Original PDF ↗
Saudi Food and Drug Authority (SFDA) · Technical Regulation
Requirements for Post-Market Surveillance of Medical Devices (MDS – REQ11)
اشتراطات المراقبة في مرحلة ما بعد طرح المنتج في السوق للأجهزة الطبية (MDS – REQ11)
Action requiredReference
The Saudi Food and Drug Authority issued requirements for post-market surveillance of medical devices (MDS – REQ11).
PublishedMarch 28, 2023
Effective—
GazetteNot gazetted
Saudi regulatory updates, in one morning brief
Bawadir tracks what Saudi regulators issue and delivers what needs your attention each working morning. Your email is all we ask for.
Free. One click to unsubscribe, any time.