Plan yoghurt pot, lid and film formats for denesting, filling, sealing, cleaning and changeover trials with representative samples.
List each pot size and specification with the lid or sealing film, target fill quantity and yoghurt variant. Use the actual format range for denesting, dosing and sealing trials, including planned format changes.
Supply representative pots, lids or film for the normal and difficult formats. Record the filling temperatures, target quantities and cleaning and changeover requirements that the agreed trial needs to cover.
Use representative product and packaging to connect pot and lidding specifications to denesting, dosing, sealing and cleaning decisions. Compare the complete format range rather than assuming one nominal sample represents the line.
Discuss your applicationDescribe how you observe or measure pot, lid and film specifications 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 pot, lid and film specifications.
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.