Trial and acceptance guide

Shrink wrapping machine sample trials and FAT

A practical framework for sample selection, process trials, factory acceptance, site commissioning and repeatable production release.

Trial preparation

Build a representative sample matrix before the formal trial

A useful sample trial or factory acceptance test proves the proposed machine against defined products, production film, operating conditions and pass/fail criteria. The test should not be used to discover basic requirements that could have been agreed beforehand.

Select process extremes, not only best sellers

Include the largest envelope, heaviest pack, least stable group, smallest product, most heat-sensitive item and strictest presentation standard. One product may represent several extremes, but the matrix should show which risk each sample covers.

Supply enough production film

Provide labelled reels or sleeves for setup, optimisation, sustained running, gaps, restart and changeover. A short unlabelled strip cannot prove reel handling, tracking, splice policy or steady production.

Freeze acceptance criteria

Agree seal condition, shrink finish, side opening, corner appearance, product condition, sleeve position, output duty and defect limits before the formal run. Use an approved pack or annotated photographs where judgement could otherwise be subjective.

Define test states and records

State warm-up, first-off, normal loading, sustained duration, production gaps, controlled faults, restart, product changes and cooling/downstream checks. Record the product, film, recipe, actual speed where verified and every deviation.

Example sample matrix structure. Replace the descriptions with the actual production range and acceptance evidence.
Sample groupReason for inclusionTest evidence
Nominal high-volume packEstablish the main production recipe and normal loadingAccepted finish, sustained good-pack output, settings and retained sample
Largest loose-film or group envelopeChallenges seal clearance, aperture, guides and transfersNo contact or catch; seal and shrink remain within standard
Heaviest or densest packChallenges conveyor support, thermal load and coolingStable transfer, tunnel recovery and acceptable product condition
Least stable groupChallenges collation, guides, airflow and dischargePattern remains controlled before, through and after shrinking
Most heat-sensitive product/label/closureDefines the lowest product tolerance within the rangeNo unacceptable deformation, marking, adhesive or closure effect
Alternative film or supplier materialConfirms whether a separate recipe or approval is requiredMaterial identity retained and result accepted under defined conditions
Changeover pairRepresents the most demanding format or material transitionDocumented change, first-off approval and return to stable output

Acceptance stages

Separate FAT, site commissioning and production release

Each stage answers a different question. The exact scope belongs in the quotation and agreed acceptance document; the framework below helps avoid assuming that one short supplier test proves every site condition.

Typical purpose of each acceptance stage. Terminology and contractual scope should be agreed for the specific project.
StagePrimary purposeEvidence
Pre-trial readinessConfirm samples, film, scope, safety, utilities and acceptance criteria are availableApproved test plan, product/film matrix and responsibilities
Supplier sample trialAssess process route and develop an application-specific proposalTrial record, photographs/video where authorised, settings and open technical points
Factory acceptance test (FAT)Demonstrate the agreed machine scope before shipment under available factory conditionsSigned test results, deviations, open-action list, manuals/documents and retained references
Site installation/commissioningConfirm access, services, assembly, interfaces and operation in the final environmentInstallation checks, line-interface tests, safety review, recipes and training records
Site acceptance/production releaseDemonstrate agreed operation with site materials, staff and line conditionsAccepted packs, sustained run, restart/changeover evidence and formal sign-off

Approve the plan

Freeze products, film, test states, defect limits, roles and records.

Run and record

Capture actual conditions, accepted output, defects, interventions and deviations.

Resolve actions

Assign every open item, owner, due condition and evidence required for closure.

Release the baseline

Retain recipes, samples, training and sign-off for repeatable production.

FAT record contents

  • Machine identity and tested configuration.
  • Product and film codes with photographs of labels and samples.
  • Approved test plan and acceptance criteria.
  • Actual settings, conveyor speed where verified, spacing and loading.
  • Run duration, accepted output and reject/defect record.
  • Production gap, restart, controlled stop and recovery results.
  • Changeover and first-off approval where included in scope.
  • Safety, guarding and functional checks defined for the FAT stage.
  • Open actions, responsible party and closure evidence.
  • Signed acceptance, retained samples, recipes and document list.

Do not treat video as the full acceptance record

A run video can demonstrate general operation but may not show actual settings, all defects, product condition or test duration. Keep the written test data and retained samples as the primary evidence.

Control deviations during the test

Record every product, film, setting or hardware change made after the plan was approved. State whether the result remains within scope or requires a separate test before shipment or site release.

Carry open actions into commissioning

An unresolved factory condition should not disappear from the project record. Assign ownership and define the evidence required at site, especially where factory utilities or adjacent equipment could not reproduce final production.

Sample trial and FAT questions

How many samples are needed for a shrink-wrapping trial?

Enough to set up, establish an accepted pack, run the agreed sustained condition, test gaps/restart and cover product extremes. The required quantity depends on the machine and test plan; agree it before shipping samples.

Should the intended production film be used?

Yes, wherever possible. Film supplier, construction, gauge, width, perforation and reel behaviour can affect sealing and shrinking, so an unlabelled substitute weakens the evidence.

Does FAT replace site acceptance?

Not necessarily. Factory conditions may not reproduce final conveyors, services, operators, environment or upstream/downstream machines. Define what is proven at FAT and what remains for commissioning or site acceptance.

What happens if a product changes after FAT?

Assess whether dimensions, weight, stability, film, heat sensitivity or acceptance have changed. A material change may require a controlled new trial or recipe rather than automatic release.

Application review

Agree samples and pass/fail evidence before the formal run

Send the product matrix, labelled production film, approved pack standard, required output, test states and sign-off responsibilities so Lancing can define a representative trial and acceptance scope.