Pharmaceutical & chemical industry

A defined degree of safety in terms of particles is required in pharmaceutical and cosmetics industry cleanrooms. The elimination of micro-organisms is what is important. In order to ensure the hygienic purity, the equipment used in the production must not bring in or distribute any impurities and must also achieve the desired result.

Medical technology

Sterility is required in every production area in which products are manufactured that will be used by people at a later point in time in order not to harm these people through contact with harmful contaminants. In medical technology it is therefore absolutely essential to eliminate micro-organic contaminations and remove, for example, germs or bacteria in production sterile rooms. In medical technology cleanrooms, the safe, efficient disinfection plays a significant role.

Semiconductor industry and optical technology

In these kinds of sensitive manufacturing areas even the smallest particles can lead to downtimes, significant quality problems and even to manufacturing stops. For this reason, the removal of particulate contaminations is of great importance. The cleaning equipment itself must not represent a source of particulate contaminations.

Foodstuffs industry

Cleanrooms in the foodstuffs industry are subject to particularly stringent requirements for mobile systems. In order to not subject the manufacturing areas to the dangers of cross-contamination and in order to be able to completely disinfect the cleanrooms, cleaning equipment and textiles are required that meet the highest hygienic standards and that deliver the best, most consistent as well as the required disinfection results. Our EasyMop GMP system has been tested and certified to this end.

Controlled area

The cleanroom technology is gaining access to an increasing number of manufacturing locations. However, not every form of product manufacturing automatically requires a cleanroom that –for regulatory reasons – follows the rules and regulations of ISO 14644, since the critical particles sizes are significantly higher than the standard maximum particle size of 5 micrometers. The assessment can follow as per VDA 19 or ISO 16232. This is where controlled areas are used. Regulations are also in place for controlled areas; for the cleaning process these mean that process-reliable approaches must apply and that the source of contamination must also be controllable in controlled areas. Our cleanroom hygiene systems fulfil these criteria.

With our systems MopFloat GMP and EasyMop GMP we have created solutions that are state of the art in cleanroom cleaning.