ISO 13485

The responsibility of a medical device manufacturer in Saudi Arabia does not end with the release of the device. According […]

Calibration being one of the significant requirements for ISO 13485 according to the Saudi Food and Drug Authority, consultants stress

One of the significant requirements in the ISO 13485 certification standard is the need for proper calibration of all medical

For medical device manufacturers in Saudi Arabia, the ISO 13485 certification is one of the required Quality Management System (QMS)

As per the requirements of the ISO 13485 certification, all involved personnel must have the requisite training, skills and competency

One of the essential requirements for any company in Saudi Arabia to achieve the ISO 13485 certification is to choose

Proper documentation is one of the essential prerequisites for ISO 13485 certification. Yet, according to most consultants this is where

ISO 13485 being one of the most important certifications for medical device manufacturers, most businesses look towards expert consultants in

The Saudi Food And Drug Authority recommends ISO 13485 as one of the required certifications for medical device manufacturers. Today

Getting the ISO 13485 certification required by the SFDA standards is one of the prerequisites for medical device manufacturers in