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Send a project brief, photos and production targets.
View optionsUse these answers to prepare a better machinery brief, then confirm the final route against representative product, containers and production targets.

An automatic filling machine transports containers through a controlled dosing process with sensors, conveyors and programmed cycles, reducing manual handling and supporting integration with closing and labelling equipment.
Liquids, oils, creams, gels, sauces, pastes, chemicals, powders and granules can all be filled automatically when the dosing principle and product-contact design match the product.
Start with product behaviour, then fill range, container, output, accuracy, cleaning and line integration. Product trials are useful where behaviour is uncertain.
A piston uses a defined cylinder displacement. Pump filling controls delivery from a selected pump. The better route depends on viscosity, particles, shear, dose range, cleaning and required motion control.
Servo filling uses programmable electric motion to control a piston, pump or nozzle axis. Recipes can store position and speed profiles for validated products and formats.
Vacuum filling draws a thin liquid into a rigid container to a set visible level. It can compensate visually for small variations in container internal volume.
Head count follows the real fill and index cycle, sustained output, product feed and downstream capacity. More heads are not useful if another station limits the line.
Often yes within an agreed size and stability range. Guide rails, nozzle positions, change parts and recipes may need adjustment.
Accuracy is product- and machine-dependent. Agree the target, reference quantity, test conditions, sample size and measurement method rather than relying on an unqualified percentage.
Yes. A complete line can include infeed, rinsing, filling, capping, sealing, labelling, coding, inspection, reject and accumulation.
Depending on the design and product, cleaning may involve draining, flushing, strip-down, manual wash, sanitisation, CIP or dedicated product-contact sets.
Samples are especially useful for foaming, sticky, stringing, particulate, abrasive, hot-fill, high-value or chemically aggressive products.
Potentially, after checking dimensions, speed, controls, emergency stops, guarding, pack transfers and available documentation.
The agreed machine scope is tested against a written protocol covering safety, operation, product and pack handling, output, fill results, faults and documentation.
Provide product data, fill range, containers, closures, target output, accuracy, cleaning, utilities, line scope, floor space and required timing.
A useful technical answer depends on the actual production conditions.
These answers help define the evidence needed for selection and fault diagnosis. Final suitability still depends on the product, pack, machine configuration and agreed trial conditions.
Trailing product can result from stringing behaviour, trapped pressure, unstable supply, an unsuitable valve or nozzle, worn seals, incorrect shut-off timing or product left in a long outlet path. Diagnose it with representative product during a sustained run, including pause and restart, rather than judging one isolated fill.
A head-to-head difference can come from feed distribution, trapped air, temperature, hose length, calibration, valve condition, nozzle restriction or the local dosing module. Take samples in head order and record the product-supply condition so a common change can be separated from a fault on one channel.
Possible controls include a stable product feed, reduced or staged delivery speed, suitable nozzle position, bottom-up movement where appropriate, controlled headspace and enough settling time for the agreed measurement. The effective combination depends on the real product, temperature, transfer method and container.
Potentially, when particle size, shape, concentration and settling behaviour are compatible with the selected pump, piston, valve, hose and nozzle. Representative samples should be tested for blockage, separation, product damage, dose consistency and clean cut-off before the route is confirmed.
CIP is suitable only when the product-contact design, cleaning chemistry, flow path and required verification support controlled circulation without leaving inaccessible areas. Other applications may be better served by flushing, strip-down cleaning or dedicated product-contact sets. The cleaning method must be specified before the machine is selected.
Compare sustained accepted packs under the same product, fill, container and line conditions. Include normal gaps, refill, planned pauses, rejects and downstream stops. A short cycle rate at the filler is not equivalent to the production output of the complete line.
Check that the approved change parts, guides, sensors, nozzle positions, recipe, labels and closure settings are fitted for the new format. Run representative first-off packs and verify container stability, fill result, neck condition, closure, label and code before releasing automatic production.
The project scope should name the physical, electrical and control boundary at every interface. It should state who supplies the transfer, which machine owns blocked and starved signals, how faults stop the line and how containers and product are recovered before restart.
Send product and pack samples, the current problem and the intended production condition so the cause can be assessed against the correct machine route.
Use the focused pages below when the answer depends on product evidence, pack handling, acceptance or the installed line rather than a general explanation.
Compare labour, run length, format change and integration.
Select dosing, nozzle and container handling as one system.
Investigate foam, stringing, cut-off and bottle-opening fit.
Prepare representative product, packs and a recorded test sequence.
Define observable acceptance and controlled deviations.
Separate common, channel and line faults, then plan spares.
Use these focused guides when a short FAQ answer is not enough to define the product, machine, line or acceptance decision.
Send the product, container, dose range, required output and known process difficulty. Lancing can identify the evidence needed before a machine route is confirmed.
Send the product, pack and output details that matter. We’ll compare the most practical dosing and line options for you.