Contact Kimberly-Clark Global Material Sourcing and Technical Support

Prepare the material brief

Name the finished product and layer function. Identify adjacent materials, bond route, fluid or particle challenge, user contact, cleanliness, care or sterilization conditions where relevant. Do not use “medical grade” or “protective” without the applicable requirement.

Provide polymer, web formation, layer sequence, basis weight and tolerance, width, treatment, surface, color and roll format. For functional evidence, include method, challenge, conditioning, specimen direction, repetitions, unit, aging and pass level.

Describe converting equipment and the planned unwind, slitting, folding, bonding, sealing or adhesive window. Include sample quantity, production volume, MOQ constraint, target date, destination and incoterm. A technically suitable web can still fail the program if roll or line requirements are not aligned.

If an earlier sample or report is referenced, give its identifier, construction, date and approval purpose. Changes in polymer, fiber, layer, basis weight, treatment or route can require renewed sampling or testing. A material report does not establish regulatory status or performance of the finished product.

For fluid-management layers, identify strike-through, rewet or absorption context and adjacent materials. For filtration, state challenge, particle range, flow, efficiency, pressure drop, loading and conditioning. For protective covers, separate flat-web barrier from seams, closures and movement.

Attach drawings only when they clarify layer stack, bond pattern, roll orientation or conversion. Unknown values can remain selection questions so the reply identifies the next sample or method. Remove unrelated confidential information.