Through a structured requirements phase, we worked closely with the customer’s production and engineering teams to understand the full scope of their operational challenges:
During the requirement analysis, we worked closely with the customer to map every packaging format they needed to support. These included foil trays and cartons—both top‑ and side‑loaded—along with the option to place leaflets either at the top or bottom of the pack.
The same primary product, such as a vial, syringe or pen/auto‑injector, could therefore require multiple packaging combinations such as:
To support very small batches, the solution also has an integrated manual packing station that maintains full GMP compliance.
This joint exploration of packaging formats gave both parties a clear view of the complexity involved and strengthened confidence that a conventional conveyor based solution would not be sufficient.
This extensive variability in formats was far beyond the capabilities of what one line with traditional transport and handling systems can offer. By contrast, the XPlanar‑based solution allows the customer to define pack formats batch‑by‑batch and adjust the sequence in which components are introduced, ensuring true scalability across current and future requirements.
Together with the customer, we designed and built a highly flexible solution based on Beckhoff’s XPlanar intelligent transport system. The floating movers and tile based modular design enabled us to create a platform that supports dynamic routing, parallel workflows and rapid format reconfiguration – capabilities not possible with traditional conveyor based systems.
The result is a compact (7,5m long), GMP aligned solution engineered specifically for the realities of modern CDMO production, where agility and compliance must go hand in hand.
1 High Operational Efficiency
Independent mover control enables multiple tasks to run in parallel, reducing cycle time per unit and ensuring that no process step becomes a bottleneck.
2. Rapid, fully compliant batch changes
Format and batch changes can be executed in under 30 minutes, including recipe change, documentation workflows and validation relevant steps.
3. Easy and controlled line clearance
A clean mechanical layout and minimised product contact surfaces make line clearance significantly faster and fully compliant with GMP expectations.
4. Fully integrated quality control
Inspection modules, vision systems and data driven quality documentation are integrated into the workflow, ensuring consistent traceability at every step.
5. Seamless introduction of future formats
Thanks to the XPlanar architecture, new formats can easily be introduced – supporting the CDMO’s long term commercial flexibility.
The implemented solution enables the customer to run small and medium batches with greatly improved efficiency, while retaining full regulatory control. It supports a scalable portfolio of product formats and gives the CDMO the manufacturing agility needed to remain competitive as client demands continue to evolve.
This project reflects our core mission at LSS: to design and build customer specific, future ready solutions that deliver measurable value in pharmaceutical production – whether for primary packaging, labelling, or specialised small batch operations.
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