Medical Devices Registration | Product Registration Qatar
Product Registration Qatar helps register medical devices with MoPH—covering classification, documentation, labeling, and post-market compliance.
INDUSTRIES
4/17/20252 min read
Medical Device Product Registration in Qatar
Supporting Innovation, Safety, and Compliance Across the Healthcare Sector
If your company manufactures or imports medical devices into Qatar, navigating the regulatory landscape is a critical step toward market entry.
The Ministry of Public Health (MoPH) in Qatar mandates strict requirements for medical device approval — covering everything from classification and labeling to documentation and post-market obligations.
At Product Registration Qatar, we help medical technology providers meet MoPH compliance standards with clarity, speed, and confidence.
What Is Considered a Medical Device in Qatar?
MoPH defines medical devices as any tool, instrument, machine, software, or material used for:
Diagnosis, prevention, or monitoring of diseases
Treatment or alleviation of health conditions
Supporting or sustaining life
Disinfection of medical environments or equipment
This includes:
Diagnostic equipment (e.g. blood pressure monitors, ECGs)
Surgical tools and implants
Hospital beds, gloves, and PPE
Home-use testing kits
Digital health and monitoring tools
Our Services for Medical Device Registration
✅ Product Classification & Regulatory Pathway
We help determine the correct device class (low-risk to high-risk) and identify the specific requirements for your product under MoPH’s guidelines.
✅ Technical File Compilation
We assist with documentation including:
Device description and labeling
Manufacturing process
Clinical evaluation or performance studies (if required)
Risk analysis and CE/FDA certification (if applicable)
✅ Labeling & Language Compliance
We ensure all packaging and manuals meet Arabic/English requirements, UDI (Unique Device Identifier), safety symbols, and storage/use instructions.
✅ Submission & Follow-Up
We manage the submission to the MoPH, coordinate directly with relevant departments, and track application status to ensure smooth registration.
✅ Post-Market Compliance
Once registered, we assist with renewal timelines, reporting changes, or incidents, and maintaining compliance across your product lifecycle.
Why Product Registration Qatar?
Familiarity with MoPH device classification & submission pathways
Experience with CE-marked and FDA-cleared products entering MENAT
Strong support for documentation review, translation, and tracking
From wearable tech to surgical equipment — we ensure your innovation reaches healthcare markets in full compliance.
🔗 Related Services
Starting your product journey? Learn why MoPH Approval is step one for compliance success.
Ready to Ensure Your Product is Fully Compliant?
Fill out the form below and let our experts guide you through label checks, formula validation, and registration—step by step.
