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Product Registration in Dubai and the UAE


Product registration in Dubai and across the UAE, handled end to end. Structured B2B support for brands, manufacturers, distributors and clinics.

On the record
File
No. 61109Licensed UAE establishment
Standing
B2B OnlyProfessional Services

Comprehensive Regulatory Support

What We Offer

Our services cover every stage of regulatory compliance. We begin with documentation review. We continue through authority submission and market approval. Ongoing compliance management follows after.

Savoy Drugstore provides end-to-end B2B regulatory services and supports the compliant supply of cosmetic, personal care, aesthetic, wellness, and professional-use products through licensed UAE channels.

Our Services

  1. 01

    UAE Product Registration

    Cosmetic and personal care product registration across the UAE. Each file is prepared for full compliance with the relevant authority.

    Required documentation typically includes a Certificate of Free Sale and product formulation data. Manufacturing facility details are also requested. Labelling must be provided in Arabic and English, with a Letter of Authorization.

    • Complete registration documentation
    • Formulation review and assessment
    • Label compliance verification
    • Safety assessment coordination
    • Certificate of conformity support
  2. 02

    Documentation Review & Preparation

    We review and prepare your regulatory documentation. Files are aligned with UAE authority requirements and international standards.

    • Technical dossier preparation
    • Product information file review
    • Ingredient documentation verification
    • Manufacturing documentation audit
    • Claims substantiation review
  3. 03

    Authority Coordination

    We liaise with the relevant UAE regulatory authorities. Coordination continues at every stage of the registration process.

    Cosmetics and personal care products are registered with Dubai Municipality. Products with medical or professional-use claims fall under MOHAP jurisdiction.

    • Direct authority communication
    • Query response management
    • Submission status tracking
    • Amendment coordination
    • Renewal management
  4. 04

    International Brand Support

    Dedicated support for international brands entering the UAE market. Local regulatory knowledge guides each step of the entry.

    • Market entry strategy
    • Local regulatory navigation
    • Cultural compliance guidance
    • Regional requirement alignment
    • Long-term market support
  5. 05

    Clinic Product Registration

    Registration support for clinics launching in-house or professional-use products. Every file is built to the applicable UAE regulatory framework.

    All medical, injectable, and professional-use products are supplied exclusively to licensed healthcare facilities and are not available for consumer retail sale, in accordance with MOHAP regulations.

    • Professional-use product registration
    • Clinic brand compliance
    • Treatment product documentation
    • Aesthetic product regulatory support
    • Private label registration
  6. 06

    Regulatory Advisory

    Ongoing advisory for end-to-end regulatory management. We help your portfolio stay compliant as requirements change.

    • Regulatory landscape monitoring
    • Compliance gap analysis
    • Strategic planning support
    • Portfolio regulatory management
    • Regulatory change notification

How cosmetic product registration works in the UAE

Product registration Dubai requirements follow the product type, not the brand. The route is decided before any file is opened. The sections below set out how cosmetic product registration works here.

Which products require registration

Product registration required in the UAE covers a broad range of goods. Cosmetic products such as skincare, colour cosmetics and haircare fall inside the scope. Personal care products, including cleansers, deodorants and oral care, are treated the same way. Professional-use preparations supplied to clinics and salons are also in scope. The product type determines the authority, the dossier and the permitted claims. Borderline formulations are classified first, before documents are gathered.

Documents needed for registration

A registration file is built from documents, not from statements. Ingredient lists must be complete, with concentrations where these are requested. Lab testing reports support safety, stability and microbiological performance. Artwork and labels are reviewed in Arabic and English. A Certificate of Free Sale from the country of origin is normally required. The trading license of the importer or local distributor is part of every submission. Missing or expired documents are the most common cause of delay.

The step by step process with the UAE authorities

The process runs in a fixed order. First, the product type is classified and the responsible UAE government authority is identified. Cosmetic and personal care products are handled by Dubai Municipality. Products carrying medical or professional-use claims fall under MOHAP and the Emirates Drug Establishment. Second, a gap analysis lists what is missing. Third, the dossier is assembled and labels are corrected. Fourth, the file is submitted and queries are answered. Timelines are estimates and depend on authority queues.

What a cosmetics registration UAE consultant does

A consultant carries the administrative load for the brand. We confirm the correct route for your products in Dubai and the wider UAE. We list every document required and check each one before filing. We correct labels and claims ahead of submission. We coordinate directly with the authority and manage queries through to closure. Registration outcomes remain with the authority, and no result or duration is guaranteed.

Our Process

Understand the Regulatory Journey

Expected duration

Dubai Municipality (Montaji) cosmetic and personal-care registration: about 1 to 2 months. MOHAP / Emirates Drug Establishment product classification: 10 working days. Manufacturer registration: approximately 4 to 6 weeks. Marketing authorisation for drugs, biopharmaceuticals and medical devices: 45 working days.Estimates, counted from the point the documentation set is complete and correct. Authority queues vary.

Our structured approach ensures clarity and transparency at every stage of the regulatory process.

Tailored to Your Requirements

Our services are tailored to meet the specific regulatory needs of each client. Contact us for a comprehensive assessment of your requirements and a structured approach to UAE market entry.