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Pharmaceutical and healthcare manufacturers require accurate product coding to support identification, quality control and traceability. In India, manufacturers of medicines, supplements, diagnostic products and medical supplies need reliable solutions for printing batch numbers, manufacturing dates, expiry dates and other variable information on packaging. Small print areas, different materials and strict quality requirements make precision particularly important.
LMI-LEIBINGER continuous inkjet printers provide non-contact coding solutions for pharmaceutical cartons, blister packaging, vials, ampoules, bottles and selected medical products. With small-character printing capabilities, specialised inks and automatic nozzle sealing technology, LMI-LEIBINGER supports clear, consistent coding while helping manufacturers reduce production interruptions.
Yes. LMI-LEIBINGER CIJ printers can print batch numbers, manufacturing dates, expiry dates and other variable information on suitable pharmaceutical packaging materials. Applications include folding cartons, selected blister foils, glass containers, plastic bottles and secondary packaging. Ink selection and print quality should be verified for the specific material.
Yes. Selected LMI-LEIBINGER printers support micro-printing for applications with limited marking space. Suitable configurations can also print machine-readable codes, including Data Matrix codes. The required code size, resolution and readability must be evaluated for the chosen printer and packaging material.
Yes. LMI-LEIBINGER CIJ printers can be integrated into automated packaging processes to apply variable information during production. Depending on the printer configuration, external systems may supply printing data. Pharmaceutical applications may additionally require appropriate validation, data management and code verification.
No. A coding printer is one component of a pharmaceutical identification process. LMI-LEIBINGER printers can apply required information, but regulatory compliance also depends on correct data, validated processes, applicable packaging requirements and any necessary inspection or serialisation systems.
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