ISO 13485 Certified
01Certified Quality Management System focused on medical devices, guaranteeing high standards and process excellence.
About Us
Empowering Compliance, Enabling Growth
Your trusted regulatory partner in the GCC and MENA regions. We are a premier consulting group specializing in seamless market access.
The MRG Advantage
The MRG Advantage
Your trusted regulatory partner in the GCC and MENA regions. We empower global manufacturers and local distributors by simplifying compliance for pharmaceuticals, medical devices, and cosmetics.
SFDA, EDE, EDA
02Fully authorized and compliant regulatory consultancy with key regional authorities ensuring trusted service delivery.
Global Manufacturer Network
03Partnering with manufacturers worldwide to streamline regulatory compliance and accelerate market access across MENA.
End-to-End Registration Support
04Extensive expertise across pharmaceuticals, medical devices, and cosmetics — from dossier preparation through post-approval lifecycle management.
Mission & Vision
The MRG promise: one partner, every regulator, across MENA.
Today
MRG's Mission
We get medical technologies approved, registered, and represented across MENA, with local teams handling every regulator, in every market, end to end.
Tomorrow
MRG's Vision
A MENA region where every safe medical innovation reaches patients without regulatory delay, with MRG as the region's definitive market-access partner.
Our Journey
A decade of regional expansion
From a single Riyadh office to a pan-MENA regulatory consultancy trusted by 1,000+ healthcare companies — explore the milestones that shaped MRG.
201201 / 05
Chapter 01
Founded in Saudi Arabia
Established as an Authorized Representative and Consultancy Company specializing in medical devices in Saudi Arabia.
201702 / 05
Chapter 02
Dubai Office
Expanded regional operations with the launch of MRG in the United Arab Emirates.
201903 / 05
Chapter 03
Cairo Office
Obtained EDA licensing for MRG in Egypt, enabling regulatory services within the Egyptian market.
202104 / 05
Chapter 04
Expanded to Pharma & Cosmetics
Secured Egyptian licensing to provide regulatory services for pharmaceuticals, medical devices, and cosmetics.
202405 / 05
Chapter 05
Regulatory & Quality Training Programs
Introduced specialized Regulatory and Quality Training Programs in Egypt to support industry professionals.
Our Team
The Minds Behind MRG
Our team combines regional expertise and global best practices to deliver personalized, expert regulatory support at every step.
Executive Leadership
Mohsen Al Muslimani
Chief Executive Officer (CEO)
Leading MRG's strategic vision and regional expansion across MENA healthcare regulatory markets.
Saudi Arabia Operations
Hamoud Al Sahli
KSA Manager
Oversees SFDA regulatory submissions and local agent services for manufacturers in the Kingdom.
Business Development
Dr. Abdulkareem Arrowsmith
Business Development Dep.
Drives strategic partnerships and market access initiatives for global healthcare manufacturers.
Regulatory Affairs
Eng. Suliman Ahmed
Regulatory Affairs Dep.
Leads technical dossier preparation and authority liaison across pharmaceuticals and devices.
Regulatory Affairs
Dr. Abdullah Alfridi
Regulatory Affairs Dep.
Specialist in post-approval compliance and lifecycle management across MENA markets.
Credentials
Certifications & Licenses
Accreditations and authority licenses that underpin our commitment to quality, compliance, and client trust.
ISO 13485:2016
Quality Management System for Medical Devices — certified quality management focused on medical devices.
International Organization for Standardization
Licensed Pharmaceutical Consulting Company
Licensed pharmaceutical consulting company with the Emirates Drug Establishment (EDE), United Arab Emirates.
EDE — United Arab Emirates
Licensed Scientific Office
Licensed Scientific Office with the Egyptian Drug Authority (EDA), Egypt (License No. 1/2022).
EDA — Arab Republic of Egypt
SFDA Consultation Office
SFDA Consultation office — CO-2023-FO-0022 for pharmaceutical, cosmetic, and medical device activities.
SFDA — Kingdom of Saudi Arabia
Why MRG
This is delivered through:
With proven expertise, global reach, and strong regional partnerships, MRG empowers healthcare companies to navigate regulatory pathways with confidence and efficiency.
0+
Manufacturers
Stat 10K+
SKU Registrations
Stat 20+
Local Companies
Stat 30+
Countries
Stat 4Company Story
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Delivered through
01
Regulatory Expertise
Helping Pharmaceutical Products, medical device, and cosmetic companies navigate approvals with ease.
02
Global Experience
Trusted by 500+ manufacturers worldwide for faster, smoother market entry.
03
Regional Authority Access
Strong partnerships with MENA regulators, including SFDA, EDA, and MoHAP.