Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices

  Click here to visit Guidance on requirements for Unique Device Identification (UDI) for Medical...
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Regulations for Personal Use Devices by SFDA

SFDA has issued a new regulation  and requirement for the personal use devices. Kindly find the link below; http://www.sfda.gov.sa/en/medicaldevices/regulations/DocLib/Reg-med-86.pdf If you require the English version of the announcement,...
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MRG is proud be to assigned by Hologic BVBA to be their Authorized Representative on behalf of the manufacture in dealing with the SFDA

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Updates on medical device marketing authorization (MDMA) procedure following United Kingdom leaving European Union (Brexit)

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Guidance on Requirements for Unique Device Identification (UDI) for Medical Devices

  Click here to visit Guidance on requirements for Unique Device Identification (UDI) for Medical...
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SFDA Announcement

Saudi Food and Drugs Authority-SFDA is working on preparing a guideline for safe and effective management of medical devices within healthcare facilities. The guideline intends to describe the best practices associated with the elements of life...
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Assessment on Guidance Criteria of Medical Devices Bundling

The Saudi Food and Drug Authority (SFDA) represented by the Medical Devices Sector (MDS), is pleased to invite interested and concerned to give their comments and views on some of the existing projects before approval. This is considered as an...
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