Get your electronic devices cleared for the UAE market without the compliance confusion. PRD manages your full TDRA Type Approval , MoIAT ECAS certification, and Customs ReleasePermit processing end-to-end so your shipments pass through customs and your devicesreach the market on schedule.
Market Opportunity:
The UAE is the commercial gateway for electronics entering the Gulfregion and wider Middle East. With world-class port infrastructure, duty-free zones like JAFZAand DAFZA, and direct trade corridors to Saudi Arabia, Oman, Kuwait, Bahrain, and Qatar, properly registered devices gain access to one of the highest per-capita electronics consumption markets in the world.
Regulatory Framework:
The UAE enforces a dual-authority compliance framework forelectronic devices. The Telecommunications and Digital Government Regulatory Authority(TDRA) governs all radio and telecom equipment, while the Ministry of Industry and Advanced Technology (MoIAT) manages safety, energy efficiency, and environmental compliance through the Emirates Conformity Assessment Scheme (ECAS). Both operate independently, and many devices require approval from each.
Business Impact:
Devices carrying valid TDRA type approval and ECAS certification gain immediate credibility with UAE distributors, retailers, and e-commerce platforms includingAmazon.ae and Noon. Without proper registration, your shipment is held at customs, your products are denied shelf access, and your brand absorbs the cost of delays, penalties, and lost market timing.
Our Team of professional advisors will contact you for a tailored package that suits your requirements
Mandatory ISO/IEC 17025 testing ensures every device meets RF emission, EMC, health exposure, and electrical safety standards before reaching UAE consumers.
Unregistered devices are seized at UAE ports. Retail, e-commerce, and B2B resale all require valid TDRA and ECAS certification.
A valid TDRA certificate is the foundation for obtaining per-shipment Customs Release Permits through Mirsal, keeping your supply chain moving.
TDRA Conformity Mark and ECAS Emirates Quality Mark on your device signal verified compliance to retailers, consumers, and regulators.
Expert evaluation to determine which regulatory authority and risk-based scheme applies toyour specific device.
Comprehensive preparation of the documentation required by TDRA and MoIAT for deviceevaluation and approval.
Complete management of the TDRA application process from submission through certificateissuance.
Dual-layer registration across MoIAT ECAS and UAE customs systems for complete marketaccess.
Most devices registered and customs-ready in 3 - 5 weeks with a structured TDRA approval workflow.
18–25 working days (depending on document readiness and testing requirements)
Traditional herbs, botanical extracts, phytochemicals, and natAED 10 per product/size (mandatory application fee) + optional AED 220 per certificateural health products
Vary based on SKU volume; discounts for bulk registrations
Device specifications reviewed to determine TDRA, ECAS, or dual-authority applicability and assign the correct risk-based scheme.
Complete technical file compiled schematics, diagrams, antenna specs, BOM, and DoC audited for discrepancies before submission.
Device samples tested at ISO/IEC 17025 accredited labs for RF, EMC, health, and safety. Scheme 3 includes TDRA in-country testing.
Notified Body audits the technical file and issues an Evaluation Report. Complete application submitted to TDRA for approval.
TDRA issues your Type Approval certificate valid for 3 years with Conformity Mark specifications for product labeling.
Conformity documentation submitted to the MoIAT ECAS portal for Emirates Quality Mark and UAE Certificate of Conformity issuance.
The process involves several regulatory steps handled through Dubai Municipality’s Montaji system:
You must have a UAE company with a valid trade license (activity: trading of detergents/disinfectants or general trading).
Without a local license, registration cannot be initiated.
Submit product artwork with full details in English & Arabic. Labels must include product name, ingredients, batch number, manufacturing & expiry date, usage instructions, and safety precautions.
Required documents include: Free Sale Certificate (from country of origin) Ingredients/Material Safety Data Sheet (MSDS) Company Trade License (UAE) Certificate of Analysis (COA) if applicable
The product is uploaded into the Dubai Municipality system for review.
Certain disinfectants (especially hospital-grade or hand sanitizers) may require laboratory testing for active ingredients and safety compliance.
Once approved, the product receives a Dubai Municipality Registration Certificate valid for importation, distribution, and sale across Dubai/UAE.
One partner for TDRA, ECAS, and customs release technical file to cleared shipment.
Every test report, DoC, and technical file audited for discrepancies before submission.
Direct relationships with TDRA-designated Notified Bodies and accredited testing laboratories.
Scheme 1, 2, or 3 correct pathway managed without misclassification delays.
Native Arabic translators deliver compliant manuals and labeling not machine translations.
Fixed-fee proposals scoped to your device portfolio. No hidden costs, no scope creep.


















EXCELLENT Based on 10 reviews Posted on Anseeya AliTrustindex verifies that the original source of the review is Google. I recently had the pleasure of registering my Product with Riz & Mona organization and I was thoroughly impressed by the efficiency and professionalism of the process. The registration was seamless, well-structured, and user-friendly. The instructions provided were very clear n concise. I highly recommend their services to anyone looking for a hassle-free experience.Posted on Hajra MirTrustindex verifies that the original source of the review is Google. The service was very amazing, and i had a great experience.Thankyou so much. Would definitely recommend this company.Posted on Nala SediegoTrustindex verifies that the original source of the review is Google. Extremely glad that I got my cosmetic product registered through your company which was professionally handled. Thank you so much!Posted on Alina AshrafTrustindex verifies that the original source of the review is Google. The services was amazing they had done the great job 👍 They registered my products and did great helped throughout the process 🌸Posted on Zaynab QuraishiTrustindex verifies that the original source of the review is Google. I booked products and i am very satisfied with the service .... thank you so much from Saudi Arabia ❤️❤️❤️Posted on Mehak KhawarTrustindex verifies that the original source of the review is Google. Had a great experiencePosted on Ammad ZafarTrustindex verifies that the original source of the review is Google. I got my product registered through your company for which im very glad that I chose your services as the procedure was seamless and very well coordinated. The professionalism and prompt responses to the client are highly commendable and I would also recommend your services to my acquaintances.Posted on Anna DevotoTrustindex verifies that the original source of the review is Google. I have done cosmetics products registration in DM , with PRD company and got all the aprovals quite easy and quick. They have big experience and helped me a lot with the necessary documents. And very important - they are always response on your messages quickly, answer on all your questions, not like many other similar companies in Dubai. Thanks a lot!! Highly recommend this company.
Get your devices cleared for the UAE market with TDRA Type Approval , MoIAT ECAScertification , and Customs Release Permits all managed end-to-end by PRD. Focus ongrowing your market share. We handle the regulatory complexity.
3 to 5 weeks from submission of a complete application. Delays typically result from incomplete documentation, DoC-to-test-report discrepancies, or in-country testing requirements under Scheme 3.
3 to 5 weeks from submission of a complete application. Delays typically result from incomplete documentation, DoC-to-test-report discrepancies, or in-country testing requirements under Scheme 3.
3 years. Renewal should be initiated well before expiry. An expired certificate means no new Customs Release Permits can be issued, effectively halting your imports.
Scheme 1 (Low Risk) Bluetooth headsets and similar devices; requires a Supplier’s Declaration of Conformity only. Scheme 2 (Medium Risk) Wi-Fi routers, GPS trackers; requires full technical documentation and accredited lab reports. Scheme 3 (High Risk) Mobile phones; requires all Scheme 2 documentation plus potential in-country TDRA lab testing.
ISO/IEC 17025 accredited lab test reports (no older than 3 years), Manufacturer’s Declaration of Conformity, complete Technical File (schematics, diagrams, antenna specs, component lists), valid UAE Trade License, GSMA TAC letter for cellular devices, and UAE Pass credentials at SOP2 or SOP3 level.
For TDRA: No. Foreign manufacturers can apply directly. For MoIAT ECAS (particularly RoHS): Yes. A local authorized representative within the UAE is typically required.
A mobile phone registered through TDRA specifically for the UAE market. Includes full local network compatibility, local manufacturer warranty, pre-installed Arabic language support, and region-specific accessories including the correct charger plug.
Devices are held at customs and denied a release permit. No post-import grace period approval must be secured before shipment arrives. Repeat violations result in fines, Mirsal blacklisting, and goods confiscation.
Yes. A separate permit is required for every shipment through Mirsal, even with valid TDRA Type Approval. Permits are issued within one working hour when documents are correct. Type approval alone does not clear customs.
The Mirsal customs system requires UAE Pass authentication. Only Advanced (SOP2) or Qualified (SOP3) accounts are accepted. Standard accounts cannot process customs declarations.
Partially. TDRA requires RF and telecom-specific testing while ECAS requires safety and energy efficiency testing so most products need separate or supplementary reports from ISO/IEC 17025 accredited labs.
An accredited entity designated by TDRA to audit technical files and issue Evaluation Reports for Scheme 2 and 3 devices. Manufacturers must select a single Notified Body per product. Entities like Intertek serve in this capacity.
Yes. TDRA devices carry the TDRA Conformity Mark with QR code. ECAS products display the Emirates Quality Mark (EQM). Both must include scannable QR codes. Consumer product manuals must include Arabic. Power plugs must meet UAE standards (Type G, 220–240V, 50Hz).
For B2B transactions involving mobile phones, computers, and accessories, the 5% VAT shifts from seller to buyer under the RCM only when the buyer is VAT-registered and intends to resell.
Depends on number of device models, scheme classification (Scheme 1 costs significantly less than Scheme 3), and testing requirements. Government fees are fixed; lab costs vary by device complexity; consultancy fees scale with portfolio size.
We’re here to help. If you didn’t find the answer you were looking for, feel free to reach out to our team. We’ll make sure you get the clarity you need to move forward with confidence.
Get fast TDRA approval, full ECAS compliance, and customs-ready documentation from technical file to cleared shipment.