مدونتنا

October 21, 2024

SFDA's Post-Market Clinical Follow-up (PMCF): Ensuring Medical Device Safety and Effectiveness

Post-Market Clinical Follow-up (PMCF) is a crucial aspect of maintaining the safety and effectiveness of medical devices after they have been introduced into the market.

October 13, 2024

Understanding Medical Device Marketing Authorization (MDMA) in Saudi Arabia

Medical Device Marketing Authorization (MDMA) ensures that medical devices entering the Saudi market meet regulatory standards set by the Saudi Food and Drug Authority (SFDA).

October 13, 2024

Saudi Arabia's Unique Device Identification (UDI) Role in Medical Device Safety

SFDA has introduced stringent regulations for Saudi-DI for all medical devices marketed within the Kingdom.

August 4, 2024

Comparing SFDA’s IVD Regulatory Framework with IVDR (European Standards)

Reliable diagnostics are essential for public health, making it imperative to understand the regulatory frameworks that govern these devices.

مدونتنا

SFDA's Post-Market Clinical Follow-up (PMCF): Ensuring Medical Device Safety and Effectiveness

SFDA's Post-Market Clinical Follow-up (PMCF): Ensuring Medical Device Safety and Effectiveness

Understanding Medical Device Marketing Authorization (MDMA) in Saudi Arabia

Saudi Arabia's Unique Device Identification (UDI) Role in Medical Device Safety

Comparing SFDA’s IVD Regulatory Framework with IVDR (European Standards)

المدونة والمقالات

آخر المقالات

SFDA's Post-Market Clinical Follow-up (PMCF): Ensuring Medical Device Safety and Effectiveness

Understanding Medical Device Marketing Authorization (MDMA) in Saudi Arabia

Saudi Arabia's Unique Device Identification (UDI) Role in Medical Device Safety

Comparing SFDA’s IVD Regulatory Framework with IVDR (European Standards)