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Medical Devices

Saudi Arabia

We provide comprehensive regulatory support for medical devices in Saudi Arabia in full compliance with SFDA requirements, covering the entire product lifecycle:

Acting as the local Authorized Representative to manage regulatory communication, submissions, and compliance obligations with SFDA.
Additionally, obtaining and supporting Medical Device Establishment Licenses (MDEL) for local manufacturers and clients operating in Saudi Arabia.

Egypt

We assist you in maneuvering through Egypt's complex regulatory processes through our EDA-licensed Scientific Office as a reliable partner to all our clients.

From the submissions of assembled registrational dossiers and approvals of submissions to the post-marketing and vigilance activities of manufacturers, we provide full support, even in the representation of manufacturers.

UAE

We provide end-to-end regulatory support in the UAE to ensure your products meet all local necessities. Our services include product registration with the Ministry of Health (MOH).

Product listing with Abu Dhabi Health Authority (HAAD) and Dubai Health Authority (DHA), as well as registering medical products with the Emirates Authority for Standardization and Metrology (ESMA).

Regulatory Affairs Consultation for the MENA Region

MRG delivers tailored regulatory affairs consultation services designed to meet the unique needs of companies operating across the MENA region. We partner with pharmaceutical, medical device, and cosmetics manufacturers to help them navigate complex regulatory landscapes and achieve smooth market entry.

Our Services

Regulatory Compliance

Expert support to ensure full alignment with local regulations, standards, and authority requirements.

Product Registration

Streamlined management of registration processes to secure timely approvals and accelerate market access.

Certifications & Licenses

  • SFDA Consultation office - CO-2023-FO-0022
  • Licensed Pharmaceutical Consulting Company — Emirates Drug Establishment (EDE), United Arab Emirates
  • Licensed Scientific Office — Egyptian Drug Authority (EDA), Egypt (License No. 1/2022)
  • ISO 13485:2016 — Quality Management System for Medical Devices
  • Ready to discuss your regulatory needs?

    Reach out today to begin your compliance journey with MRG.

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