Build an evidence request around the intended claim

The RFQ should separate microbiological evidence from product compatibility and marketing review.

Intended statement
What to record: Exact antibacterial, odour-control or hygiene wording and placement
Project detail: ____________________
How to confirm: Review wording for destination market before artwork approval

Assessment scope
What to record: Target organisms, method, contact time and reporting format
Project detail: ____________________
How to confirm: Agree the laboratory protocol and report fields

Treated construction
What to record: Fibre, weave, shade, finish route and treated side
Project detail: ____________________
How to confirm: Link sample code and report to the exact material version

Care history
What to record: Cleaning chemistry, temperature, drying and required cycle point
Project detail: ____________________
How to confirm: Prepare specimens through the specified sequence before assessment

Product compatibility
What to record: Colour, hand, odour, sewing, buckle travel, adjacent materials
Project detail: ____________________
How to confirm: Compare treated and untreated assembly samples

Material identification
What to record: Order code, label and untreated-stock separation
Project detail: ____________________
How to confirm: Check purchase documents, packaging and retained sample

A material assessment does not by itself justify a medical, health-protection or permanent-effect claim.

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