Medical device companies to be ISO 13485 certified in Saudi Arabia

ISO 13485 certification involves preparation of the

1 . Regulatory requirements stated by SFDA Saudi Food and Drug Authority

2. Preparation of the Medical Device File MDF

3. Identifying the right ISO Standard to carry out Risk assessment of the Medical device.

4. Training your staff based on the ISO 13485 standards

5. Preparation of your company for ISO 13485 SFDA Approved certifications

Email at [email protected] to know more about ISO 13485 SFDA certification or for SFDA ISO 13485 Consultants in Riyadh, Jeddah, Dammam, Jubail, Yanbu, Hofuf

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