In This Guide
  1. What the Reform Actually Changes
  2. The Three Domains Covered
  3. How the Route Works
  4. Benefits for Importers
  5. What Still Must Be Done
  6. Limits & Exclusions
  7. Frequently Asked Questions

1. What the Reform Actually Changes

For decades, a product legally sold across the European Union still had to go through a separate Israeli approval process — often duplicative, often more expensive than the product itself, and always slower. A European toy, a European appliance, a European cosmetic that had passed every EU safety requirement could sit in a bonded warehouse in Ashdod for weeks while Israeli-specific lab testing was repeated.

The 1 January 2025 reform writes the EU directive directly into the Israeli regulatory path. A product demonstrably compliant with the applicable EU directive — evidenced by CE marking, a manufacturer's Declaration of Conformity (DoC), the Technical File, and the relevant harmonised-standard test reports — can be imported to Israel on that basis. A duplicate Israeli certification is no longer required by default.

2. The Three Domains Covered

The reform is a single policy framework that applies across three distinct regulatory domains. Each has its own sector ministry, its own acceptance mechanism, and its own documentation — but all share the same principle of EU equivalence.

Domain Regulator EU basis
Standardisation (electrical, EMC, machinery, toys, construction, etc.) Ministry of Economy — Commissioner of Standardisation CE-marked products under harmonised directives (LVD, EMCD, Machinery, Toy Safety, RED, MDR...)
Food Ministry of Health — Food Service Products compliant with EU food law (Food Information to Consumers Regulation, additives, contaminants, labelling)
Cosmetics Ministry of Health — Pharmaceutical Division Products compliant with the EU Cosmetics Regulation (EC) 1223/2009 and CPNP notification

Each domain has a dedicated guide — see our food imports guide and cosmetics imports guide for the specifics.

3. How the Route Works

In all three domains, the practical mechanism is the same three-step pattern:

  1. Evidence of EU compliance. The manufacturer or the EU importer of record holds the documentation package required under the EU directive — CE marking for industrial products, CPNP notification for cosmetics, EU labelling for food. The importer in Israel obtains copies of this package.
  2. Israeli declaration and registration. The importer in Israel declares — under legal responsibility — that the product complies with the referenced EU directive, and registers the declaration with the relevant Israeli authority (a pre-approval for food, a notification for cosmetics, or an importer declaration under the standardisation reform).
  3. Israeli-specific adaptations. Hebrew labelling, Hebrew instructions / safety information, Israeli electrical plug where relevant, and compliance with the Israeli grid (230V/50Hz — which matches EU). None of these replace the EU directive; they are localisation layers on top.

4. Benefits for Importers

5. What Still Must Be Done

The reform replaces duplicate certification, not Israeli-specific localisation. Several requirements apply regardless of EU compliance:

6. Limits & Exclusions

The reform does not cover everything. Key exclusions:

Frequently Asked Questions

What is the "What's Good for Europe is Good for Israel" reform?
A cross-ministry Israeli regulatory reform, effective 1 January 2025, that accepts EU-directive compliance as sufficient basis for import into Israel — eliminating duplicate Israeli certification in three domains: standardisation (electrical, machinery, toys, EMC, etc.), food, and cosmetics. A product demonstrably compliant with the relevant EU directive can be imported with an importer declaration instead of a separate Israeli lab approval.
Does this reform make CE marking sufficient for Israel?
For products under harmonised EU directives — Low Voltage (LVD), Electromagnetic Compatibility (EMCD), Machinery, Toy Safety, Radio Equipment (RED), Medical Devices (MDR) and similar — yes, CE marking backed by the full compliance documentation (Declaration of Conformity, Technical File, harmonised standard test reports) is the basis for Israeli acceptance. Products not covered by a harmonised directive still go through the traditional Israeli-standard track.
Is Hebrew labelling still required?
Yes. The reform replaces duplicate certification, not Israeli-specific localisation. Hebrew labelling of product name, manufacturer, importer of record, warnings, and usage instructions remains required under the Consumer Protection Law and sector-specific rules. The same applies to Hebrew safety information, Israeli plug compatibility, and any Israeli-specific on-product markings.
Does the reform apply to products from outside the EU?
It applies to products that comply with EU directives, not necessarily to products manufactured in the EU. A Chinese-manufactured appliance that has been tested and certified under the EU Low Voltage Directive with a CE marking and full compliance file can be imported into Israel under the reform. What matters is the EU compliance, not the country of manufacture.
What if the product is recalled in the EU?
If the EU itself recalls, bans, or withdraws the product — for example through the Safety Gate / RAPEX rapid alert system — the Israeli acceptance falls away. The importer must stop imports and may face recall requirements in Israel. Monitoring EU safety-notice channels is an operational requirement for importers using the reform.
Does the reform reduce customs duty or VAT?
No. The reform is a regulatory-compliance reform, not a tax reform. Customs duty, purchase tax, and VAT continue to apply under their normal rules. For duty reduction on EU origin, the separate EU-Israel Association Agreement and the Pan-Euro-Med cumulative origin system remain the relevant mechanisms — see our Import Taxation guide.
Source: Ministry of Economy, Ministry of Health — "What's Good for Europe is Good for Israel" reform (effective 1 January 2025); Commissioner of Standardisation procedures; EU New Legislative Framework harmonised directives (LVD 2014/35/EU, EMCD 2014/30/EU, Machinery Directive 2006/42/EC, Toy Safety Directive 2009/48/EC, RED 2014/53/EU, MDR 2017/745, Cosmetics Regulation (EC) 1223/2009, FIC Regulation (EU) 1169/2011); Israeli Ministry of Economy import guide (gov.il).
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