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Quality & documents

Verification is a process, not a badge.

Our launch quality framework follows a clear chain, designed so trade partners can understand what is specified, tested and documented.

The process

1

Product specification

The range is being developed against a clear specification.

2

Batch identification

The planned release process includes batch identification linked through packing and source records.

3

Independent testing

Independent analytical testing is being built into the launch specification, with results reported as measured.

4

Clear documentation

The documentation set will be matched to the product, batch and destination-market requirements.

Commercial documentation

A clear document set for commercial release.

Documentation will be aligned to the selected product, production partner and destination market before commercial orders are accepted.

Product specification
Defined for the selected product and format
Launch standard
Batch test result (as measured)
Independent analytical results reported as measured
Launch standard
Certificate of Analysis (COA)
From the accredited testing process
Launch standard
Origin & traceability records
Batch code linked back to source
Launch standard
Packaging details
Confirmed with the packer
Format-specific
Shelf life
Product-specific
Destination / market documents
Depends on the destination country
Destination-dependent
Final documents are issued against the confirmed product and destination

Our line

Quality, never a health claim.

We describe what we test as compositional quality grades — the way the industry does — and never attach a therapeutic or medical outcome.

Trade & distribution

Trade and distribution enquiries are welcomed from selected international markets. Tell us about your market and requirements.