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ESMA Certification in the UAE: ECAS, EQM and G-Mark Explained

There is no single 'ESMA certificate'. ECAS is mandatory conformity for market access; EQM is a voluntary quality mark; G-Mark is GCC-wide. Getting the distinction wrong is expensive.

Businesses ask how to get an ESMA certificate. The honest first answer is that there isn’t one — there are several schemes, they do different jobs, and buying the wrong one is a common and expensive mistake.

First, the name

The Emirates Authority for Standardization and Metrology (ESMA) was the federal standards body. Its functions now sit within the Ministry of Industry and Advanced Technology (MoIAT).

The schemes continue under MoIAT, and “ESMA” remains in common use — including in tender documents and customer requirements written years ago. If a client asks for “ESMA certification,” they mean one of the following, and it is worth establishing which before anyone quotes.

The schemes, and which one you need

ECAS EQM G-Mark
Full name Emirates Conformity Assessment Scheme Emirates Quality Mark Gulf Conformity Mark
Mandatory? Yes, for regulated products No — voluntary Yes, for products in scope
Purpose Legal market access in the UAE Demonstrating quality Market access across GCC states
Assesses Product conformity to technical regulations Product and the factory’s management system Product conformity to GCC technical regulations
Typical output Certificate of Conformity Right to use the EQM mark Right to apply the G-Mark

ECAS is the one most businesses actually need. If your product falls under a UAE technical regulation, you cannot legally import, distribute or sell it without conformity assessment. This is not optional and not a marketing decision.

EQM is voluntary, and heavier. It assesses your factory and quality management system as well as the product, and typically requires an ISO 9001 management system in place. It exists to demonstrate quality, not to grant market access. Pursuing EQM when the requirement was ECAS means paying for a considerably larger assessment than the regulation demanded.

G-Mark operates at GCC level, covering categories including low-voltage electrical equipment and toys. If you sell across the Gulf rather than only in the UAE, this is the relevant route.

Some businesses need more than one — ECAS for legal access, EQM because a retailer or government buyer asks for it.

Which products are regulated

Technical regulations apply to specific categories, and the list changes. Categories commonly in scope include:

  • Electrical and electronic products
  • Cosmetics and personal care products
  • Food contact materials
  • Construction and building materials
  • Automotive products and components
  • Household appliances
  • Toys
  • Chemicals and detergents

Check the current regulation for your specific product rather than relying on a category list — including this one. Scope is defined by technical regulation and HS code, and a product that looks like it belongs in a category may not be in scope, or may be in scope under a regulation you did not expect.

The process

  1. Determine applicability. Which technical regulation covers your product, and which scheme follows from it. Getting this wrong at step one wastes everything after it.
  2. Testing. Against the standards named in the regulation, at a laboratory accepted for the purpose. Test reports from a laboratory not recognised under the scheme will not be accepted, however competent the lab.
  3. Technical documentation. Product specification, test reports, risk assessment, manufacturing details, quality control arrangements, labelling and markings.
  4. Application through the relevant MoIAT system.
  5. Factory assessment, where the scheme requires it — always for EQM, sometimes for ECAS depending on the regulation and conformity assessment route.
  6. Certificate issued, valid for a defined period with renewal and, for some schemes, surveillance.

Where applications fail

  • Wrong scheme identified at the start, so the assessment does not match the regulatory requirement
  • Test reports from a laboratory not accepted under the scheme
  • Incomplete technical documentation, particularly around traceability from the tested sample to the production product
  • Labelling and marking non-compliance — correct product, wrong markings
  • Product changed after certification without notification, invalidating the certificate

The last one is the most costly, because it usually surfaces at the border.

One thing to check about any provider

Conformity assessment bodies operating under these schemes are notified or registered by MoIAT for defined scopes. As with any accreditation, the scope matters — a body recognised for one product category is not thereby recognised for yours.

Ask any provider which scheme and which product categories they are recognised for, and verify it rather than accepting the answer.

The same distinction between assessment and consultancy applies here as elsewhere: a body assessing your product’s conformity should not also be the party preparing your compliance case. If one provider offers to do both, ask how they maintain impartiality.

Common questions

Is it still called ESMA? The authority’s functions moved to MoIAT, but the scheme names — ECAS, EQM, G-Mark — remain in use, and “ESMA” persists informally and in older documents.

Do we need ECAS or EQM? ECAS if your product is regulated and you need market access. EQM only if you want the quality mark, or a customer requires it. They are not alternatives to each other.

How long is a certificate valid? Defined by scheme and product category, with renewal required. Changes to the product, manufacturer or specification need notifying.

We are certified in another country. Does that count? Not automatically. UAE technical regulations set their own requirements, though existing test reports may be usable depending on the laboratory’s recognition and the standards applied.

What happens without certification? Regulated products without valid conformity assessment can be held at the border, refused entry, or removed from sale. It is a market access requirement, not a formality.


Ask about product certification — tell us your product and HS code and we will confirm which scheme applies before quoting. See product certification and product testing.

This article is provided for information only and does not constitute professional or compliance advice. ITMAD accepts no liability for any action taken in reliance on it.