In 2010, we redesigned our entire production facility to meet increasing client demands, and since then we’ve been producing labels, labelling products and labelling systems under GMP conditions in the clean room. The protected area is entered via a hygiene sluice and meets category 8 clean room conditions as stipulated in ISO 14644-1. The continuous clean room monitoring includes ongoing measurement of the air particles and positive air pressure in the room, the air exchange rate, room temperature and relative humidity. Lines are completely cleared and in-process controls are carried out at all stages in the manufacture of semi-finished and finished products. At the end of the process, tests and final checks are conducted before the products are sent to the packaging area.

All processes are carried out and monitored in accordance with ISO 9001. This certainly isn’t the usual way that labels are produced. Since the products to be labelled have to meet the highest standards worldwide, so should the labelling.