Agree yoghurt variants, pot and lid formats, target quantities, production conditions and the method used to check fills, seals and finished packs.
Agree representative yoghurt variants, filling temperatures, pot and lid or film formats, target fill quantities and production conditions before the trial. Record how fill quantity, the seal area and the finished pack will be judged.
Define normal, difficult and fault conditions, planned format changes and cleaning requirements. Agree the acceptable result, the record to keep and the response when a finished pack falls outside the agreed range.
Use the agreed trial method, repetitions, acceptable range and result record to assess the complete pot denesting, dosing and sealing route. Keep the production team validation responsibilities clear.
Discuss your applicationDescribe how you observe or measure finished-pack checks and reject handling in your operation, including sample condition and any measuring limits. For a project focused on yoghurt pot filling and lidding, also record the production state in which each observation was made.
For Yoghurt Pot Fillers, include normal production conditions, credible extremes, product or part variants and changes over time.
Show which settings, safeguards, maintenance tasks, decisions or required outcomes are affected by changes in finished-pack checks and reject handling.
State the yoghurt variants and filling temperatures to be used in the trial. Include representative normal and difficult samples and any product differences the filling and lidding trial must cover.
Provide the actual pot sizes and specifications, together with the lids or sealing film. Include the full format range for the pot denesting and sealing trials.
State the target fill quantity for each pot format and the finished-pack checks needed to confirm the result during trials.
Describe routine output requirements, short runs and planned format changes so the agreed trial reflects the production pattern the line must handle.
Set out cleaning, allergen and product changeover requirements. Include access needs and identify the production team validation responsibilities.
Trial pot denesting, dosing and sealing together with representative product and packaging. Check the seal area and finished pack using an agreed method, acceptable range and result record.