MRG is proud to be assigned by “NIBEC Co. Ltd” as their Authorized Representative to deal on behalf of the manufacture with the Saudi Food And Drug Authority “SFDA

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SFDA Announcement about postponing the new medical devices marketing authorization fees.

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

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SFDA Announcement about postponing the new medical devices marketing authorization fees.

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MRG is proud to be assigned by “Adoderm GmbH” 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 assigned by “eSight Corporation” as their Authorized Representative to deal on behalf of the manufacture with the Saudi Food And Drug Authority “SFDA”

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Come visit us at Hall 7a B09 at Medica Trade Fair – Dusseldorf Germany

To know more about our company and its services during Medica Trade Fair at Dusseldorf, Germany. Kindly email us at munzer@mr-gate.com to schedule a...
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SFDA – DRAFT Guidelines for Innovative Medical devices

For More Information about the DRAFT Guidelines for Innovative Medical Devices, please visit https://www.sfda.gov.sa/ar/medicaldevices/regulations/DocLib/G-InnovativeMD-Finalized.pdf For And inquiries or suggestion, please fill in the below link or...
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MRG is proud to be assigned by “Sysmex Corporation” 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 assigned by ‘Matoke Holding Limited’ 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 assigned by ‘Crawford Healtcare Ltd’ 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 assigned by “NIBEC Co. Ltd” as their Authorized Representative to deal on behalf of the manufacture with the Saudi Food And Drug Authority “SFDA

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SFDA Announcement about postponing the new medical devices marketing authorization fees.

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

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New SFDA Unified Portal

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

For more information, please...
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Come visit us at Hall 7a B09 at Medica Trade Fair – Dusseldorf Germany

To know more about our company and its services during Medica Trade Fair at Dusseldorf, Germany. Kindly email us at munzer@mr-gate.com to schedule a...
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MRG is proud to be assigned by “OsteoCare Dental Implants Solutions” as their Authorized Representative to deal on behalf of the manufacture with the Saudi Food And Drug Authority “SFDA”

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SFDA – DRAFT Guidelines for Innovative Medical devices

For More Information about the DRAFT Guidelines for Innovative Medical Devices, please visit https://www.sfda.gov.sa/ar/medicaldevices/regulations/DocLib/G-InnovativeMD-Finalized.pdf For And inquiries or suggestion, please fill in the below link or...
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MRG is proud to be assigned by ‘Matoke Holding Limited’ 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 assigned by ‘X-Nav Technologies, LLC’ as their Authorized Representative to deal on behalf of the manufacture with the Saudi Food And Drug Authority ‘SFDA’

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SFDA Announcement about the Guidance on requirements for reporting of incident and Adverse event of medical devices (MDS-G39)

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SFDA Announcement on the Latest Update Of Medical Device Marketing Authorization (MDMA) fees

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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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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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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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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 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 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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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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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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Draft Guidance of New Registration Requirements For Medical Devices.

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

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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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