MRG is proud to be assigned by “Matricel” as their Authorized Representative to deal on behalf of the manufacture with the Saudi Food And Drug Authority ‘SFDA’

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MRG is proud to be recommended by Mr. Orlando Antunes, Director Regulatory Affairs EMEA from Zimmer Biomet for MRG’s excellent services and support towards the company.

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MRG is proud to be assigned by BlueGrass Vascular as their Authorized Representative to deal on behalf of the manufacture with the Saudi Food And Drug Authority

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SFDA announcement about update on requirements for importation of laboratory products for general use

For more information, please click: https://www.sfda.gov.sa/ar/medicaldevices/circulations/DocLib/SDFA-MD215515.pdf For information about the Guidance on requirements of shipments, please...
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SFDA announcement about updated timeframe for deleting medical device marketing authorization (MDMA) application

Click here for more information: https://www.sfda.gov.sa/ar/medicaldevices/circulations/DocLib/SDFA-MDSAN015.pdf...
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Update of medical devices marketing authorization fees

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MRG is proud to be assigned by ProMedica Bioelectronic Sr as their Authorized Representative to deal on behalf of the manufacture with the Saudi Food And Drug Authority

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SFDA Announcement about Blood Collection bags and Renal Dialysis Solutions

Click here for more information: https://www.sfda.gov.sa/ar/oper/circulations/DocLib/oper62058.pdf...
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MRG is Proud to be assigned by “Santen OY” as their Authorized Representative to deal on behalf of the manufacture in dealing with the Saudi Food And Drug Authority (SFDA)

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MRG is Proud to be assigned by “Stratpharma AG” as their Authorized Representative to deal on behalf of the manufacture in dealing with the Saudi Food And Drug Authority (SFDA)

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MRG Proudly announces signing with “Norav Medical GmbH “, to be their Official Authorized Representative in KSA.

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Implementations of additional requirements for breast implant devices

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Draft Guidance of New Registration Requirements For Medical Devices.

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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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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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