Certification Process

Eight clear steps to kosher certification

Every operation is different, but the route to certification should be understandable. KAG uses a structured review to connect your application with real products and production conditions.

The KAG pathway

From first review to continued assurance

The sequence below describes a normal industrial certification pathway. The exact timing and evidence depend on scope, complexity and readiness.

01

Application

Share your company, facility, products and commercial objectives so KAG can define the scope of review.

02

Product & ingredient review

KAG reviews formulations, raw materials, suppliers and supporting certificates relevant to the proposed certified products.

03

Facility assessment

Production flows, equipment, storage, utilities and shared-line conditions are assessed against kosher requirements.

04

Certification review

Findings are evaluated and any required ingredient, process or control changes are documented clearly.

05

Agreement & approval

The certification scope, approved products, operating conditions and ongoing responsibilities are confirmed in writing.

06

Certification authorization

Once conditions are met, KAG authorizes the approved products within the defined certification scope.

07

Label & mark approval

Packaging that will display the KAG mark is reviewed before use so the mark appears only on authorized products.

08

Ongoing compliance

Periodic review, renewal and change control help keep ingredients, products, sites and labels aligned with the certification.

Prepare well

What helps the review move efficiently

Complete, consistent information reduces avoidable follow-up and lets the assessment focus on material certification questions.

  • A defined product and facility list
  • Current formulas, ingredients and supplier details
  • Process flows and shared-equipment information
  • A company contact who can coordinate quality, purchasing and production
Timing

How long does certification take?

There is no responsible universal timeline. The number of products and sites, formula complexity, supplier documentation, facility scheduling and any required changes all affect completion.

SCOPE

Products and sites

A focused, accurate initial scope is easier to evaluate than an undefined portfolio.

READINESS

Documents available

Current supplier and process information can prevent repeated clarification cycles.

COMPLEXITY

Shared operations

Multi-use equipment and co-manufacturing arrangements may need deeper review.

ACTIONS

Changes required

Ingredient replacements or operating controls must be resolved before approval.

Next step

Ready for the first step?

Submit a practical overview of your company, products and facilities. KAG will use it to define the review scope.

Apply for Certification